510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K142814Substantially Equivalent

Biomet Orthopaedic Salvage System (OSSTM) - Proximal Femoral & Hybrid Tibial

Biomet Manufacturing Corp, Warsaw IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K142814 is the FDA 510(k) clearance record for Biomet Orthopaedic Salvage System (OSSTM) - Proximal Femoral & Hybrid Tibial, a class II device, cleared for Biomet Manufacturing, LLC on under FDA product code JDI (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented). FDA records list 128 510(k) clearances for Biomet Manufacturing, LLC, from to . As of , FDA records show 6 recalls naming K142814.

Clearance record

Decision date
Received
(269 days to decision)
Product code
JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
Regulation
21 CFR 888.3350
Device class
Class II
Review panel
Orthopedic
Applicant
Biomet Manufacturing, LLC 56 E Bell Dr., Warsaw IN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JDI

Trailing 12 months
3 clearances under product code JDI in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JDI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20261
August 20261
September 20260
October 20260