K242871
- 510(k) number
- K242871
- Device name
- ATTUNE Revision Hinge Knee
- Applicant
- Depuy Ireland UC IE
- Product code
- KRO — Prosthesis, Knee, Femorotibial, Constrained, Cemente
- Decision date
- 2024-11-21
- Date received
- 2024-09-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K242871.pdf
Official FDA record: K242871
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.