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FDA 510(k) Applications Submitted by SYNTHES (USA) PRODUCTS, LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K172157
07/18/2017
DePuy Synthes Femoral Recon Nail System
Synthes (USA) Products, LLC
K160167
01/27/2016
DePuy Synthes TFNA Augmentation System
Synthes (USA) Products, LLC
K170802
03/17/2017
TRAUMACEMÖ V+ Injectable Bone Cement
Synthes (USA) Products, LLC
K131548
05/30/2013
SYNTHES TROCHANTERIC FIXATION NAIL - ADVANCED SYSTEM
SYNTHES (USA) PRODUCTS, LLC
K150099
01/20/2015
Depuy Synthes Variable Angle Locking Hand System (1.3 mm and 2.0 mm Plates and Screws)
SYNTHES (USA) PRODUCTS, LLC
K180213
01/25/2018
Titanium TomoFix Medial High Tibia Plate Anatomical
Synthes (USA) Products, LLC
K182154
08/09/2018
Depuy Synthes Femoral Neck System
Synthes (USA) Products, LLC
K180544
03/01/2018
DePuy Synthes Static Staples
Synthes (USA) Products, LLC
K150796
03/26/2015
Dental Bone Cutting Instruments
SYNTHES (USA) PRODUCTS, LLC
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