PolyLock Midfoot CD-CA-1050
PolyLock Midfoot CD-CA-1050 is a Class I device made by Fusion Orthopedics, LLC, cleared under FDA 510(k) K211843 on 4 Mar 2022 and listed in FDA GUDID since 2 Oct 2025 (UDI-DI 00840124521872), 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 | Number00840124521872 | Date2 Oct 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK211843 | Date4 Mar 2022 | StatusActive |
Official records
- AccessGUDID record 00840124521872
- FDA 510(k) database K211843
Across registries
- FDA 510(k) K211843 decided 4 Mar 2022 Active
- FDA GUDID UDI-DI 00840124521872 listed 2 Oct 2025 Listed
Timeline
- Cleared FDA 510(k) K211843
- Listed FDA GUDID 00840124521872
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- PolyLock Midfoot
- Generic name
- Orthopaedic bone pin, non-bioabsorbable
- Model / Ref / Catalog
- CD-CA-1050
- Primary DI / UDI-DI
- 00840124521872
- 510(k) Number
- FDA product code
- HXQ
- GMDN term
- Orthopaedic bone pin, non-bioabsorbable
- Device class
- Class I
- Regulation number
- 888.4540
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization