Product code KRP
- Device name
- Prosthesis, Knee, Patello/Femorotibial, Constrained, Cemented, Polymer/Metal/Metal
- Medical specialty
- Orthopedic
- Device class
- 3
- Regulation number
- 888.3550
- Review panel
- OR
- Implant
- Y
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Definition
- Call for PMAs to be filed by 12/26/96 per 61 FR 50710 on 9/27/96
- Source
- FDA openFDA device classification dataset