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

Platform® Acetabular System

K Number: K220483 · Decision Sep 23, 2022
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
21
Review Days
217

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Basic Information

Device Name
Platform® Acetabular System
K Number
K220483
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Total Joint Orthopedics, Inc.
Date Received
February 18, 2022
Decision Date
September 23, 2022
Product Code
LZO
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
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

Similar 510(k) Clearances

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

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Other Clearances by Total Joint Orthopedics, Inc.

K Number Device Name
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
K180159 Klassic® Knee 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. →