Alamo C 2016T-212
Alamo C 2016T-212 is a Class I device made by Alliance Partners LLC, cleared under FDA 510(k) K173128 on 22 Mar 2018 (1 earlier submission) and listed in FDA GUDID since 23 Sep 2016 (UDI-DI M6862016T2120), 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 | NumberM6862016T2120 | Date23 Sep 2016 | StatusListed |
Official records
- FDA 510(k) database K173128
- FDA 510(k) database K133321
Across registries
- FDA 510(k) K173128 decided 22 Mar 2018 Active
- FDA GUDID UDI-DI M6862016T2120 listed 23 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K133321
- Listed FDA GUDID M6862016T2120
- 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- Withdrawn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
- Spinal implant trial
- Model / Ref / Catalog
- 2016T-212
- Primary DI / UDI-DI
- M6862016T2120
- FDA product code
- HTR, HWT
- GMDN term
- Spinal implant trial
- Device class
- Class I
- Regulation number
- 878.4800, 888.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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