PROPEL C8600
GUDID 30845854014831
9 MM X 20 MM PROPEL CANNULATED INTERFERENCE SCREW
Conmed Corporation
Tendon/ligament bone anchor, non-bioabsorbable| Primary Device ID | 30845854014831 |
| NIH Device Record Key | 94ba5b6d-c8b7-4731-a4f2-28a1145aaaca |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PROPEL |
| Version Model Number | C8600 |
| Catalog Number | C8600 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 1 |
| 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
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 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10845854014837 [Previous] |
| GS1 | 20845854014834 [Primary] |
| GS1 | 30845854014831 [Package] Contains: 20845854014834 Package: Box [1 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K874676
FDA Product Code
| HWC | Screw, fixation, bone |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-04-15 |
| Device Publish Date | 2024-04-05 |
On-Brand Devices [PROPEL]
| 20845854015343 | 9MM X 25MM PROPEL INTERFERENCE SCREW |
| 20845854015305 | 8MM X 30MM PROPEL INTERFERENCE SCREW |
| 20845854015237 | 8MM X 20MM PROPEL INTERFERENCE SCREW |
| 20845854015220 | 8MM X 25MM PROPEL CANNULATED INTERFERENCE SCREW |
| 20845854015213 | 7MM X 30MM PROPEL CANNULATED INTERFERENCE SCREW |
| 20845854015190 | 9MM X 30MM PROPEL INTERFERENCE SCREW |
| 20845854015084 | 8MM X 25MM PROPEL INTERFERENCE SCREW |
| 20845854015060 | 9MM X 30MM PROPEL CANNULATED INTERFERENCE SCREW |
| 20845854014957 | 7MM X 25MM PROPEL INTERFERENCE SCREW |
| 20845854014919 | 7MM X 20MM PROPEL INTERFERENCE SCREW |
| 20845854014797 | 9MM X 20MM PROPEL INTERFERENCE SCREW |
| 20845854014780 | 7MM X 20MM PROPEL CANNULATED INTERFERENCE SCREW |
| 20845854014766 | 8MM X 30MM PROPEL CANNULATED INTERFERENCE SCREW |
| 20845854014636 | 7MM X 30MM PROPEL INTERFERENCE SCREW |
| 20845854014629 | 8MM X 20MM PROPEL CANNULATED INTERFERENCE SCREW |
| 20845854014612 | 7MM X 25MM PROPEL CANNULATED INTERFERENCE SCREW |
| 20845854014483 | 9MM X 25MM PROPEL CANNULATED INTERFERENCE SCREW |
| 10845854014837 | 9MM X 20MM PROPEL CANNULATED INTERFERENCE SCREW |
| 30845854014831 | 9 MM X 20 MM PROPEL CANNULATED INTERFERENCE SCREW |
Trademark Results [PROPEL]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PROPEL 98794068 not registered Live/Pending |
Propel, Inc. 2024-10-10 |
 PROPEL 98745882 not registered Live/Pending |
CUETEC CO., LIMITED 2024-09-11 |
 PROPEL 98625025 not registered Live/Pending |
HCPro LLC 2024-06-28 |
 PROPEL 98385072 not registered Live/Pending |
Les Composites Motion Inc. 2024-01-31 |
 PROPEL 98384146 not registered Live/Pending |
Lydonia Technologies, LLC 2024-01-31 |
 PROPEL 98102956 not registered Live/Pending |
The Visibility Company 2023-07-26 |
 PROPEL 97917479 not registered Live/Pending |
Seachem Laboratories, Inc. 2023-05-02 |
 PROPEL 97804321 not registered Live/Pending |
Propel Holdings, LLC 2023-02-21 |
 PROPEL 97766658 not registered Live/Pending |
ENGS Commercial Finance Co 2023-01-24 |
 PROPEL 97662890 not registered Live/Pending |
Vita-Mix Management Corporation 2022-11-07 |
 PROPEL 97657300 not registered Live/Pending |
Saietta Group PLC 2022-11-01 |
 PROPEL 97636421 not registered Live/Pending |
Stokely-Van Camp, Inc. 2022-10-18 |
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