CoLink® P73 ST312
CoLink® P73 ST312 is a Class II device made by Conmed Corporation, cleared under FDA 510(k) K181113 on 15 Jun 2018 and listed in FDA GUDID since 3 Jul 2025 (UDI-DI 00810021867427), active as of 22 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 | Number00810021867427 | Date3 Jul 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK181113 | Date15 Jun 2018 | StatusActive |
Official records
- AccessGUDID record 00810021867427
- FDA 510(k) database K181113
Across registries
- FDA 510(k) K181113 decided 15 Jun 2018 Active
- FDA GUDID UDI-DI 00810021867427 listed 3 Jul 2025 Listed
Timeline
- Cleared FDA 510(k) K181113
- Listed FDA GUDID 00810021867427
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- CoLink®
- Generic name
- Orthopaedic bone screw (non-sliding)
- Model / Ref / Catalog
- P73 ST312
- Primary DI / UDI-DI
- 00810021867427
- 510(k) Number
- FDA product code
- HWC
- GMDN term
- Orthopaedic bone screw (non-sliding)
- Device class
- Class II
- Regulation number
- 888.3040
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Radiation Sterilization
- MRI safety
- MR Conditional
- Size
- Width — 3.5 MillimeterLength — 12 Millimeter
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