Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Total Joint Othopedics, Inc.

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7
Categories3
Latest FDA decision2025-03-24
TypeNumberDevice NameCodeDateActions
510(k) K243991 Klassic Knee System - Revision Tibial BaseplateJWH2025-03-24 View
510(k) K232414 Klassic® Tibial Insert, PS-Post, Klassic All Poly Tibia, PS-PostJWH2023-09-08 View
510(k) K230537 Klassic Knee Revision SystemJWH2023-05-19 View
510(k) K213580 Adapter Sleeve for BIOLOX® OPTION Femoral Head, +10.5mm head lengthLZO2021-12-03 View
510(k) K191399 BIOLOX CONTOURA Ceramic Femoral HeadLZO2019-08-28 View
510(k) K171962 Klassic HD® Hip SystemLPH2017-07-24 View
510(k) K161073 Klassic HD Hip SystemLPH2016-10-19 View