510(k) K182574

Freedom Ultra-Congruent CR Tibial Liner by Maxx Orthopedics, Inc. — Product Code JWH

K182574 is an FDA 510(k) premarket notification submitted by Maxx Orthopedics, Inc. for the device "Freedom Ultra-Congruent CR Tibial Liner". The FDA issued a decision of Substantially Equivalent on January 22, 2019. 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. Maxx Orthopedics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 22, 2019
Date Received
September 18, 2018
Clearance Type
Special
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