K241491
- 510(k) number
- K241491
- Device name
- Blueprint Patient-Specific Instrumentation; Shoulder iD Primary Reversed Glenoid
- Applicant
- Stryker Corporation (Tornier, S.A.S.) FR
- Product code
- PHX — Shoulder Prosthesis, Reverse Configuration
- Decision date
- 2024-10-10
- Date received
- 2024-05-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.9 MB · U.S. public domain
Also available from FDA: K241491.pdf
Official FDA record: K241491
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.