Peri-Loc 73802316
Peri-Loc 73802316 is a Class II device made by Smith & Nephew, Inc., cleared under FDA 510(k) K210837 on 29 Jun 2021 (1 earlier submission) and listed in FDA GUDID since 21 Sep 2015 (UDI-DI 00885556142370), 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 | FDA 510(k)SESE | NumberK210837 | Date29 Jun 2021 | StatusActive |
| United States | GUDID listing | Number00885556142370 | Date21 Sep 2015 | StatusListed |
Official records
- AccessGUDID record 00885556142370
- FDA 510(k) database K210837
- FDA 510(k) database K082516
Across registries
- FDA 510(k) K210837 decided 29 Jun 2021 Active
- FDA GUDID UDI-DI 00885556142370 listed 21 Sep 2015 Listed
Timeline
- Cleared FDA 510(k) K082516
- Listed FDA GUDID 00885556142370
- Cleared FDA 510(k) K210837
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Peri-Loc
- Generic name
- Orthopaedic bone screw, non-bioabsorbable, sterile
- Model / Ref / Catalog
- 73802316
- Primary DI / UDI-DI
- 00885556142370
- FDA product code
- HWC
- GMDN term
- Orthopaedic bone screw, non-bioabsorbable, sterile
- Device class
- Class II
- Regulation number
- 888.3040
- GUDID distribution status
- In Commercial Distribution
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