K241097
- 510(k) number
- K241097
- Device name
- Arthrex Virtual Implant Positioning (VIP) System Software
- Applicant
- Arthrex, Inc. FL · US
- Product code
- QHE — Shoulder Arthroplasty Implantation System
- Decision date
- 2024-10-02
- Date received
- 2024-04-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K241097.pdf
Official FDA record: K241097
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.