K242253
- 510(k) number
- K242253
- Device name
- JARVIS Glenoid Reverse Shoulder Prosthesis
- Applicant
- FH Industrie FR
- Product code
- PHX — Shoulder Prosthesis, Reverse Configuration
- Decision date
- 2024-11-25
- Date received
- 2024-07-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K242253.pdf
Official FDA record: K242253
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.