PROPEL C8945
GUDID 20845854015305
8MM X 30MM PROPEL INTERFERENCE SCREW
Conmed Corporation
Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable| Primary Device ID | 20845854015305 |
| NIH Device Record Key | 8301b882-49fd-4716-b338-600e62f5d47b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PROPEL |
| Version Model Number | C8945 |
| Catalog Number | C8945 |
| 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
Device Dimensions
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
| Length | 30 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10845854015308 [Package] Package: Box [1 Units] In Commercial Distribution |
| GS1 | 20845854015305 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K933352
FDA Product Code
| HWC | Screw, fixation, bone |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-10-24 |
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]
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