Total Joint Othopedics, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Total Joint Othopedics, Inc. has 8 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Latest FDA clearance: Mar 2025. Active since 2014. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Total Joint Othopedics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Arthroplasty Regulatory Consulting as regulatory consultant.
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