510(k) K143725

Consensus Knee System Modular Tibial Baseplate by Consensus Orthopedics, Inc. — Product Code JWH

K143725 is an FDA 510(k) premarket notification submitted by Consensus Orthopedics, Inc. for the device "Consensus Knee System Modular Tibial Baseplate". The FDA issued a decision of Substantially Equivalent on March 4, 2015. The device falls under product code JWH (Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer), a Class II device regulated under 21 CFR 888.3560. Consensus Orthopedics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 4, 2015
Date Received
December 29, 2014
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