Alamo T
by Alliance Partners LLC 2 variants
510(k) K120401
Alamo T is a Class II device made by Alliance Partners LLC, cleared under FDA 510(k) K120401 on 5 Oct 2012, active as of 22 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)SESE | NumberK120401 | Date5 Oct 2012 | StatusActive |
Official records
- FDA 510(k) database K120401
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MAX
- FDA applicant
- Alliance Partners, LLC
- Device class
- Class II
- Regulation
- 21 CFR Part 888.3080
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent