Alamo C 1412T-300
Alamo C 1412T-300 is a Class I device made by Alliance Partners LLC, cleared under FDA 510(k) K173128 on 22 Mar 2018 (2 earlier submissions) and listed in FDA GUDID since 23 Sep 2016 (UDI-DI M6861412T3000), 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) | NumberK173128 | Date22 Mar 2018 | StatusActive |
| United States | GUDID listing | NumberM6861412T3000 | Date23 Sep 2016 | StatusListed |
Official records
- FDA 510(k) database K173128
- FDA 510(k) database K133321
- FDA 510(k) database K112361
Across registries
- FDA 510(k) K173128 decided 22 Mar 2018 Active
- FDA GUDID UDI-DI M6861412T3000 listed 23 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K112361
- Cleared FDA 510(k) K133321
- Listed FDA GUDID M6861412T3000
- Cleared FDA 510(k) K173128
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Alamo C
- Generic name
- Orthopaedic implant impactor, reusable
- Model / Ref / Catalog
- 1412T-300
- Primary DI / UDI-DI
- M6861412T3000
- FDA product code
- HWA
- GMDN term
- Orthopaedic implant impactor, reusable
- Device class
- Class I
- Regulation number
- 888.4540
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization