K223833
- 510(k) number
- K223833
- Device name
- Exactech® Equinoxe® Reverse Humeral Liners and Humeral Adapter Trays
- Applicant
- Exactech, Inc. FL · US
- Product code
- PHX — Shoulder Prosthesis, Reverse Configuration
- Decision date
- 2023-09-14
- Date received
- 2022-12-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K223833.pdf
Official FDA record: K223833
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.