Conmed 8972S
Conmed 8972S is a Class II device made by Conmed Corporation, cleared under FDA 510(k) K933352 on 23 Feb 1994 and listed in FDA GUDID since 24 Oct 2015 (UDI-DI 10845854016329), 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 | Number10845854016329 | Date24 Oct 2015 | StatusListed |
| United States | FDA 510(k)SN | NumberK933352 | Date23 Feb 1994 | StatusActive |
Official records
- AccessGUDID record 10845854016329
- FDA 510(k) database K933352
Across registries
- FDA 510(k) K933352 decided 23 Feb 1994 Active
- FDA GUDID UDI-DI 10845854016329 listed 24 Oct 2015 Listed
Timeline
- Cleared FDA 510(k) K933352
- Listed FDA GUDID 10845854016329
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- Withdrawn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
- 8972S
- Primary DI / UDI-DI
- 10845854016329
- 510(k) Number
- FDA product code
- HWC
- GMDN term
- Tendon/ligament bone anchor, non-bioabsorbable
- Device class
- Class II
- Regulation number
- 888.3040
- GUDID distribution status
- In Commercial Distribution
- Size
- Outer Diameter — 7 MillimeterLength — 30 Millimeter
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