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FDA 510(k) Applications Submitted by Amnon Talmor
FDA 510(k) Number
Submission Date
Device Name
Applicant
K080331
02/06/2008
SYNTHES CRANIOFACIAL PLATE AND SCREW SYSTEM
SYNTHES (USA)
K100634
03/05/2010
SYNTHES MATRIX SYSTEM
SYNTHES (USA)
K181060
04/23/2018
Solitaire 2 and Solitaire Platinum Revascularization Device
Medtronic Neurovascular
K221531
05/26/2022
ClotTriever Thrombectomy System
Inari Medical, Inc.
K081623
06/10/2008
SYNTHES RIB FIXATION SYSTEM
SYNTHES (USA)
K081700
06/17/2008
SYNTHES (USA) STERNAL FIXATION SYSTEM - LINE EXTENSION
SYNTHES (USA)
K071738
06/26/2007
EXACTECH OPTETRAK PROXIMAL TIBIAL SPACER
EXACTECH, INC.
K211990
06/28/2021
Rist 071 Radial Access Guide Catheter
Micro Therapeutics, Inc., d/b/a ev3 Neurovascular
K062273
08/07/2006
SPACER-G TEMPORARY HIP PROSTHESIS
TECRES SPA
K082335
08/14/2008
SYNTHES MATRIXMANDIBLE PLATE AND SCREW SYSTEM
SYNTHES (USA)
K162760
09/30/2016
Spine Wave Anterior Cervical Spine System
SPINE WAVE, INC.
K083439
11/20/2008
SYNTHES EPOCA SHOULDER PROSTHESIS SYSTEM
SYNTHES (USA)
K063569
11/29/2006
EQUINOXE REVERSE SHOULDER SYSTEM
EXACTECH, INC.
K093762
12/07/2009
SYNTHES ZERO-P
SYNTHES SPINE
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