510(k) K212941
K212941 is an FDA 510(k) premarket notification submitted by Encore Medical, L.P. Dba Djo Surgical for the device "Porous Patella". The FDA issued a decision of Substantially Equivalent on Jan 20, 2022. The device falls under product code MBH (Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer), a Class II device regulated under 21 CFR 888.3565.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jan 20, 2022
- Date Received
- Sep 15, 2021
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
- Device Class
- Class II
- Regulation Number
- 888.3565
- Review Panel
- OR
- Submission Type
- 510(k)