FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Klassic® Knee System

K Number: K180159 · Decision Mar 9, 2018
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
21
Review Days
49

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Basic Information

Device Name
Klassic® Knee System
K Number
K180159
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Total Joint Orthopedics, Inc.
Date Received
January 19, 2018
Decision Date
March 9, 2018
Product Code
JWH
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JWH), ordered by most recent decision date.

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Other Clearances by Total Joint Orthopedics, Inc.

K Number Device Name
K220483 Platform® Acetabular System
K211877 Klassic Knee System
K211602 Klassic Knee System
K202740 Klassic Knee System Tibial Inserts, PS-Max
K183596 Klassic Knee System - Klassic Knee PS-Post Femur; Klassic Knee Tibial Insert, PS-Post, Std Poly; Klassic Knee Tibial Insert, PS-Post, E-Link Poly
K190280 Klassic Knee System - Sombrero Patella with Standard Poly, Klassic Knee System - Sombrero Patella with E-Link Poly
K180929 Klassic HD® Hip System
K173104 Klassic HD® Hooded Acetabular Insert with E-Link® Poly, Klassic HD® Low Profile Acetabular Insert with E-Link® Poly
K162422 Klassic Knee System
K162256 Klassic Femur, Porous, Klassic Tibial Baseplate, Porous
Search all 21 clearances from Total Joint Orthopedics, Inc. →