Alamo C 1714T-210
Active
510(k)
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k) | NumberK173128 | Date22 Mar 2018 | StatusActive |
| United States | GUDID listing | NumberM6861714T2100 | Date23 Sep 2016 | StatusListed |
Official records
- FDA 510(k) database K173128
- FDA 510(k) database K133321
Recalls
No FDA recalls found in the data synced 23 Oct 2026.
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- Withdrawn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
- 1714T-210
- Primary DI / UDI-DI
- M6861714T2100
- FDA product code
- HWT, HTR
- GMDN term
- Spinal implant trial
- Device class
- Class I
- Regulation number
- 888.4800, 878.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Other devices from Alliance Partners LLC
Properties
Other properties (12)
- Supplied sterile: No
- Single use: No
- Implantable: No
- Contains latex: No
- Over-the-counter: No
- Convenience kit: No
- Combination product: No
- HCT/P: No
- Premarket exempt: No
- Serial number: No
- Expiration date: No
- Manufacturing date: No