K242603
- 510(k) number
- K242603
- Device name
- MyPAO SA guides
- Applicant
- Medacta International S.A. CH
- Product code
- PBF — Orthopaedic Surgical Planning And Instrument Guides
- Decision date
- 2025-11-19
- Date received
- 2024-08-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K242603.pdf
Official FDA record: K242603
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.