Identifiers
- 510(k) Number
- K133321 FDA 510(k)
- FDA Product Code
- ODP FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 888.3080 FDA 510(k)
- Regulation Number
- 888.3080 FDA 510(k)
- Advisory Committee
- Orthopedic FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Alamo C by Alliance Partners Llc — Class II — listed in FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (0 countries)
Regulatory Authorizations
No authorizations listed.
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Alliance Partners Llc
- FDA Applicant
- Alliance Partners, LLC
Sources (1)
- FDA 510(k) K133321 24 fields · synced Jun 1, 2026