510(k) K173884

Unity Total Knee System by Corin U.S.A. Limited — Product Code JWH

K173884 is an FDA 510(k) premarket notification submitted by Corin U.S.A. Limited for the device "Unity Total Knee System". The FDA issued a decision of Substantially Equivalent on Jan 17, 2018. 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. Corin U.S.A. Limited has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Jan 17, 2018
Date Received
Dec 21, 2017
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