FDA 510(k) Applications Submitted by Biomet Inc.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K212435	08/04/2021	Comprehensive Humeral Fracture Positioning Sleeves	Biomet Inc.
K183162	11/15/2018	Affixus Hip Fracture Nail	Biomet Inc.
K173767	12/11/2017	A. L. P. S. Clavicle Plating System	Biomet Inc.
K193533	12/20/2019	WIN Flexible Nail System	Biomet Inc.
K193092	11/06/2019	TunneLoc Tibial Fixation Device	Biomet Inc.
K193402	12/06/2019	ALLthread PEEK Suture Anchor	Biomet Inc.
K171540	05/26/2017	Refobacin Bone Cement R	Biomet Inc.
K193214	11/21/2019	WasherLoc and No-Profile Screw and Washer Systems, Biomet Cannulated Screw System, Biomet Headless Compression and Twist-Off Screws	Biomet Inc.
K143543	12/15/2014	Prelude PF Patellae	BIOMET INC.
K193546	12/20/2019	Distal Centralizers	Biomet Inc.
K193373	12/05/2019	Comprehensive« Reverse Shoulder	Biomet Inc.
K210192	01/25/2021	A.L.P.S. Clavicle Plating System	Biomet Inc.
K191459	06/03/2019	JuggerStitch Meniscal Repair Device	Biomet Inc.
K173278	10/13/2017	ToggleLoc System	Biomet Inc.
K192942	10/18/2019	ALLthread Titanium Suture Anchor	Biomet Inc.
K193451	12/13/2019	Titanium Interference Screws	Biomet Inc.