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FDA 510(k) Applications Submitted by STACEY BONNELL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K130146
01/22/2013
SYNTHES SYNFLATE VERTEVRAL BALLOON SYSTEM
SYNTHES (USA) LLC
K090549
03/02/2009
SYNTHES SYNAPSE TRANSCONNECTOR
SYNTHES SPINE
K211051
04/08/2021
DePuy Synthes 2.7mm Straight and 2.7mm Adaption Plates (Modular Mini Fragment LCP System)
DePuy Synthes
K091159
04/21/2009
SYNTHES ORACLE PLATE
SYNTHES SPINE
K201321
05/18/2020
DePuy Synthes 2.7mm VA LCP Clavicle Plate System
DePuy Synthes
K161417
05/23/2016
DePuy Synthes MAXFRAME Multi-Axial Correction System
SYNTHES USA, LLC
K091689
06/10/2009
SYNAPSE SYSTEM 4.0MM, OC FUSION SYSTEM 4.0MM
SYNTHES (USA)
K071667
06/19/2007
SYNTHES VECTRA-ONE SYSTEM
SYNTHES SPINE
K201959
07/14/2020
DePuy Synthes 2.7mm VA LCP Clavicle Hook Plate System
DePuy Synthes
K112068
07/20/2011
SYNTHES ZERO-P VARIABLE ANGLE (VA)
SYNTHES SPINE CO.LP
K112459
08/26/2011
SYNTHES ZERO-P
SYNTHES SPINE CO.LP
K072791
10/01/2007
ORACLE SPACER, OPAL SPACER
SYNTHES SPINE
K203414
11/19/2020
DePuy Synthes 2.7mm VA LCP Clavicle Plate System, DePuy Synthes 2.7mm VA LCP Clavicle Hook Plate System
DePuy Synthes
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