510(k) K211004

GMK Spherika Femurs and Fixed Tibial Trays Plus by Medacta International S.A. — Product Code JWH

K211004 is an FDA 510(k) premarket notification submitted by Medacta International S.A. for the device "GMK Spherika Femurs and Fixed Tibial Trays Plus". The FDA issued a decision of Substantially Equivalent on May 13, 2021. 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. Medacta International S.A. has 207 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 13, 2021
Date Received
Apr 2, 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
510(k)