Alamo P 2811T-1002
Alamo P 2811T-1002 is a Class I device made by Alliance Partners LLC, cleared under FDA 510(k) K122047 on 4 Sep 2012 and listed in FDA GUDID since 30 Sep 2016 (UDI-DI M6862811T10020), 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 | NumberM6862811T10020 | Date30 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK122047 | Date4 Sep 2012 | StatusActive |
Official records
- FDA 510(k) database K122047
Across registries
- FDA 510(k) K122047 decided 4 Sep 2012 Active
- FDA GUDID UDI-DI M6862811T10020 listed 30 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K122047
- Listed FDA GUDID M6862811T10020
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Alamo P
- Generic name
- Orthopaedic inorganic implant inserter/extractor, reusable
- Model / Ref / Catalog
- 2811T-1002
- Primary DI / UDI-DI
- M6862811T10020
- 510(k) Number
- FDA product code
- LXH
- GMDN term
- Orthopaedic inorganic implant inserter/extractor, reusable
- Device class
- Class I
- Regulation number
- 888.4540
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under Orthopaedic inorganic implant inserter/extractor, reusable.