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FDA 510(k) Applications Submitted by OSTEOMED
FDA 510(k) Number
Submission Date
Device Name
Applicant
K140978
04/16/2014
OSTEOMED LOW PROFILE ORBITAL FLOOR PLATE SYSTEM
OSTEOMED
K203479
11/27/2020
ExtremiLOCK Lateral Ankle Fusion Plates
OsteoMed
K140283
02/04/2014
OSTEOMED EXTREMIFUSE SYSTEM
OSTEOMED
K133437
11/07/2013
1ST MTP PLATE
OSTEOMED
K161041
04/13/2016
OsteoMed ExtremiLOCK Wrist Plating System
OSTEOMED
K162542
09/12/2016
OsteoMed PINNACLE Driver
OSTEOMED
K162544
09/12/2016
OsteoMed PINNACLE Driver
OSTEOMED
K130412
02/19/2013
OSTEOMED EXTREMIFUSE SYSTEM
OSTEOMED
K121304
05/01/2012
OSTEOMED CRANIAL DISTRACTION SYSTEM
OSTEOMED
K151195
05/04/2015
OsteoMed IMF Screw
OSTEOMED
K152145
08/03/2015
OsteoMed ExtremiLOCK Wrist Plating System
OSTEOMED
K131851
06/21/2013
OSTEOMED NEURO RONGEUR
OSTEOMED
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