Alamo C 0100-1412
Alamo C 0100-1412 is a Class II device made by Alliance Partners LLC, cleared under FDA 510(k) K173128 on 22 Mar 2018 and listed in FDA GUDID since 18 Apr 2018 (UDI-DI M686010014120), 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 | NumberM686010014120 | Date18 Apr 2018 | StatusListed |
| United States | FDA 510(k) | NumberK173128 | Date22 Mar 2018 | StatusActive |
Official records
- FDA 510(k) database K173128
Across registries
- FDA 510(k) K173128 decided 22 Mar 2018 Active
- FDA GUDID UDI-DI M686010014120 listed 18 Apr 2018 Listed
Timeline
- Cleared FDA 510(k) K173128
- Listed FDA GUDID M686010014120
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Alamo C
- Generic name
- Polymeric spinal interbody fusion cage
- Model / Ref / Catalog
- 0100-1412
- Primary DI / UDI-DI
- M686010014120
- 510(k) Number
- FDA product code
- ODP
- GMDN term
- Polymeric spinal interbody fusion cage
- Device class
- Class II
- Regulation number
- 888.3080
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Length — 12 MillimeterWidth — 14 MillimeterHeight — 12 Millimeter