510(k) K954909

PROFIX POSTERIOR-STABILIZED KNEE SYSTEM by Smith & Nephew Richards, Inc. — Product Code JWH

K954909 is an FDA 510(k) premarket notification submitted by Smith & Nephew Richards, Inc. for the device "PROFIX POSTERIOR-STABILIZED KNEE SYSTEM". The FDA issued a decision of SN on January 31, 1996. 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. Smith & Nephew Richards, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
January 31, 1996
Date Received
October 25, 1995
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