K260102
- 510(k) number
- K260102
- Device name
- Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System
- Applicant
- Stryker Corporation (Tornier, Inc.) MN · US
- Product code
- PHX — Shoulder Prosthesis, Reverse Configuration
- Decision date
- 2026-06-12
- Date received
- 2026-01-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
510(k) Summary (official FDA PDF): K260102.pdf
Official FDA record: K260102
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.