Conmed C2612
Conmed C2612 is a Class II device made by Conmed Corporation, cleared under FDA 510(k) K954682 on 9 Feb 1996 and listed in FDA GUDID since 10 Dec 2015 (UDI-DI 20845854019402), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number20845854019402 | Date10 Dec 2015 | StatusListed |
| United States | FDA 510(k)SN | NumberK954682 | Date9 Feb 1996 | StatusActive |
Official records
- AccessGUDID record 20845854019402
- FDA 510(k) database K954682
Across registries
- FDA 510(k) K954682 decided 9 Feb 1996 Active
- FDA GUDID UDI-DI 20845854019402 listed 10 Dec 2015 Listed
Timeline
- Cleared FDA 510(k) K954682
- Listed FDA GUDID 20845854019402
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Conmed
- Generic name
- Tendon/ligament bone anchor, non-bioabsorbable
- Model / Ref / Catalog
- C2612
- Primary DI / UDI-DI
- 20845854019402
- 510(k) Number
- FDA product code
- HTN
- GMDN term
- Tendon/ligament bone anchor, non-bioabsorbable
- Device class
- Class II
- Regulation number
- 888.3030
- GUDID distribution status
- In Commercial Distribution
- Size
- Outer Diameter — 6.5 MillimeterLength — 35 Millimeter
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