K233481
- 510(k) number
- K233481
- Device name
- AltiVate Reverse® Glenoid
- Applicant
- Encore Medical L.P. TX · US
- Product code
- PHX — Shoulder Prosthesis, Reverse Configuration
- Decision date
- 2024-05-29
- Date received
- 2023-10-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K233481.pdf
Official FDA record: K233481
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.