FDA 510(k) Applications Submitted by DIANA TAYLOR

FDA 510(k) Number Submission Date Device Name Applicant
K130140 01/22/2013 INTRA-LOCK OP DENTAL IMPLANT INTRA-LOCK INTERNATIONAL
K200538 03/03/2020 Skeletal Dynamics Forearm Plating System Skeletal Dynamics, Inc.
K200701 03/18/2020 Skeletal Dynamics Midshaft Humerus Plating System Skeletal Dynamics, Inc.
K011191 04/19/2001 MEROCEL CORNELL LID AND LASH GUARD, MEROCEL AND KEROCEL OPHTHALMIC SPONGES MEDTRONIC XOMED, INC.
K071551 06/06/2007 QUICKBRIDGE TM CYLINDER AND CAP BIOMET 3I, INC.
K051556 06/13/2005 ACUMATCH A-SERIES CONNEXION GXL ENHANCED CROSSLINKED POLYTHYLENE EXACTECH, INC.
K201662 06/19/2020 REDUCT« Headless Compression Screw System Skeletal Dynamics, Inc.
K141840 07/08/2014 TRABECULAR METAL TIBIAL CONE BROACH, TRABECULAR METAL COUPLED TIBIAL CONE BROACH ZIMMER, INC.
K201962 07/15/2020 Skeletal Dynamics Ulnar Shortening Plating System Skeletal Dynamics, Inc.
K172343 08/02/2017 Fortilink« Interbody Fusion (IBF) System with TETRAfuse« 3D Technology RTI Surgical, Inc.
K062274 08/07/2006 SPACER-K TEMPORARY KNEE SPACER WITH GENTAMICIN, MODELS SPK0021, SPK0121, SPK0221, SPK0321 TECRES SPA
K072363 08/23/2007 NANOTITE PREVAIL,CERTAIN,PARELLEL WALLED,TAPERED,EXTERNAL HEX BIOMET 3I, INC.
K072642 09/18/2007 BIOMET 3I DENTAL ABUTMENTS AND RESTORATIVE COMPONENTS BIOMET 3I, INC.
K163673 12/27/2016 FortilinkÖ-C with TETRAfuseÖ 3D Technology RTI Surgical, Inc.


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