K260721
- 510(k) number
- K260721
- Device name
- Tornier Perform Advanced Glenoid
- Applicant
- Tornier, Inc. MN · US
- Product code
- KWS — Prosthesis, Shoulder, Semi-Constrained, Metal/Polyme
- Decision date
- 2026-07-22
- Date received
- 2026-03-05
- 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: K260721.pdf
Official FDA record: K260721
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.