Peri-Loc 71801807
Peri-Loc 71801807 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 25 Aug 2015 (UDI-DI 03596010573810), 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 | Number03596010573810 | Date25 Aug 2015 | StatusListed |
Official records
- AccessGUDID record 03596010573810
- FDA 510(k) database K210837
- FDA 510(k) database K061352
Across registries
- FDA 510(k) K210837 decided 29 Jun 2021 Active
- FDA GUDID UDI-DI 03596010573810 listed 25 Aug 2015 Listed
Timeline
- Cleared FDA 510(k) K061352
- Listed FDA GUDID 03596010573810
- 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- Withdrawn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 fixation plate, non-bioabsorbable
- Model / Ref / Catalog
- 71801807
- Primary DI / UDI-DI
- 03596010573810
- FDA product code
- HRS
- GMDN term
- Orthopaedic fixation plate, non-bioabsorbable
- Device class
- Class II
- Regulation number
- 888.3030
- GUDID distribution status
- In Commercial Distribution
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