K252141
- 510(k) number
- K252141
- Device name
- AltiVate Reverse® Glenoid
- Applicant
- Encore Medical L.P. TX · US
- Product code
- PHX — Shoulder Prosthesis, Reverse Configuration
- Decision date
- 2025-08-05
- Date received
- 2025-07-08
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K252141.pdf
Official FDA record: K252141
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.