510(k) K013031
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 7, 2001
- Date Received
- September 10, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
- Device Class
- Class II
- Regulation Number
- 888.3510
- Review Panel
- OR
- Submission Type