510(k) K211602
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 23, 2021
- Date Received
- May 24, 2021
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
- Device Class
- Class II
- Regulation Number
- 888.3560
- Review Panel
- OR
- Submission Type