K234056
- 510(k) number
- K234056
- Device name
- canturio® se (Canturio Smart Extension)
- Applicant
- Canary Medical USA, LLC CA · US
- Product code
- QPP — Implantable Post-Surgical Kinematic Measurement Knee
- Decision date
- 2024-04-24
- Date received
- 2023-12-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K234056.pdf
Official FDA record: K234056
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.