Total Joint Othopedics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Klassic Knee System - Revision Tibial Baseplate, Klassic® Tibial Insert, PS-Post, Klassic All Poly Tibia, PS-Post, Klassic Knee Revision System
8
Total
8
Cleared
0
Denied
FDA 510(k) Regulatory Record - Total Joint Othopedics, Inc. Orthopedic ✕
8 devices
Cleared
Mar 24, 2025
Klassic Knee System - Revision Tibial Baseplate
Orthopedic
88d
Cleared
Sep 08, 2023
Klassic® Tibial Insert, PS-Post, Klassic All Poly Tibia, PS-Post
Orthopedic
29d
Cleared
May 19, 2023
Klassic Knee Revision System
Orthopedic
81d
Cleared
Dec 03, 2021
Adapter Sleeve for BIOLOX® OPTION Femoral Head, +10.5mm head length
Orthopedic
23d
Cleared
Aug 28, 2019
BIOLOX CONTOURA Ceramic Femoral Head
Orthopedic
96d
Cleared
Jul 24, 2017
Klassic HD® Hip System
Orthopedic
24d
Cleared
Oct 19, 2016
Klassic HD Hip System
Orthopedic
184d
Cleared
Dec 23, 2014
Klassic HD Hip System
Orthopedic
25d