C-WIRE 5050-042
GUDID 20845854029098
C-WIRE PAK DOUBLE ENDED ORTHOPAEDIC WIRE, SPADE, .035 INCH (0.89MM), QTY 50
Conmed Corporation
Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable| Primary Device ID | 20845854029098 |
| NIH Device Record Key | 47366da6-2041-4931-8abc-102e04413454 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | C-WIRE |
| Version Model Number | 00505004200 |
| Catalog Number | 5050-042 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 50 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Dimensions
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
| Length | 0.89 Millimeter |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00845854029094 [Unit of Use] |
| GS1 | 10845854029091 [Primary] |
| GS1 | 20845854029098 [Package] Contains: 10845854029091 Package: BOX [50 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K142134
FDA Product Code
| HTY | PIN, FIXATION, SMOOTH |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2023-05-25 |
| Device Publish Date | 2015-12-14 |
On-Brand Devices [C-WIRE]
| 20845854033330 | C-WIRE PAK DOUBLE ENDED ORTHOPAEDIC WIRE, TROCAR, .045 INCH (1.14MM), QTY 5 |
| 20845854033316 | C-WIRE PAK DOUBLE ENDED ORTHOPAEDIC WIRE, SPADE, .035 INCH (0.89MM), QTY 5 |
| 20845854033309 | C-WIRE PAK DOUBLE ENDED ORTHOPAEDIC WIRE, TROCAR, .062 INCH (1.57MM), QTY 50 |
| 20845854033293 | C-WIRE PAK DOUBLE ENDED ORTHOPAEDIC WIRE, TROCAR, .028 INCH (0.71MM), QTY 50 |
| 20845854033286 | C-WIRE PAK DOUBLE ENDED ORTHOPAEDIC WIRE, SPADE, .045 INCH (1.14MM), QTY 50 |
| 20845854029173 | C-WIRE PAK DOUBLE ENDED ORTHOPAEDIC WIRE, TROCAR, .062 INCH (1.57MM), QTY 5 |
| 20845854029166 | C-WIRE PAK DOUBLE ENDED ORTHOPAEDIC WIRE, TROCAR, .035 INCH (0.89MM), QTY 5 |
| 20845854029159 | C-WIRE PAK DOUBLE ENDED ORTHOPAEDIC WIRE, SPADE, .062 INCH (1.57MM), QTY 5 |
| 20845854029142 | C-WIRE PAK DOUBLE ENDED ORTHOPAEDIC WIRE, SPADE, .045 INCH (1.14MM), QTY 5 |
| 20845854029135 | C-WIRE PAK DOUBLE ENDED ORTHOPAEDIC WIRE, SPADE, .028 INCH (0.71MM), QTY 5 |
| 20845854029128 | C-WIRE PAK DOUBLE ENDED ORTHOPAEDIC WIRE, TROCAR, .045 INCH (1.14MM), QTY 50 |
| 20845854029111 | C-WIRE PAK DOUBLE ENDED ORTHOPAEDIC WIRE, TROCAR, .035 INCH (0.89MM), QTY 50 |
| 20845854029104 | C-WIRE PAK DOUBLE ENDED ORTHOPAEDIC WIRE, SPADE, .062 INCH (1.57MM), QTY 50 |
| 20845854029098 | C-WIRE PAK DOUBLE ENDED ORTHOPAEDIC WIRE, SPADE, .035 INCH (0.89MM), QTY 50 |
| 20845854029081 | .028INCH (0.71MM) PAK DOUBLE ENDED ORTHOPAEDIC WIRE, C-WIRE SPADE, QTY 50 |
| 20845854033323 | C-WIRE PAK DOUBLE ENDED ORTHOPAEDIC WIRE, TROCAR, .028 INCH (0.71MM), QTY 5 |
Trademark Results [C-WIRE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 C-WIRE 75428391 not registered Dead/Abandoned |
LINVATEC CORPORATION 1998-02-03 |
 C-WIRE 73099619 1066656 Dead/Expired |
CONCEPT, INC. 1976-09-13 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.