K241873
- 510(k) number
- K241873
- Device name
- OsseoFit Stemless Shoulder System
- Applicant
- Zimmer, Inc. IN · US
- Product code
- PKC — Prosthesis, Total Anatomic Shoulder, Uncemented Meta
- Decision date
- 2024-12-11
- Date received
- 2024-06-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K241873.pdf
Official FDA record: K241873
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.