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FDA 510(k) Applications Submitted by BLESSON ABRAHAM
FDA 510(k) Number
Submission Date
Device Name
Applicant
K210016
01/04/2021
Integra DigiFuse Cannulated Intramedullary Fusion System,Integra Total Foot System,Integra CAPTURE Screw System & Integra Ti6 Internal Fixation System,Subtalar MBA System,MetaSurg Subtalar Implant,NewDeal BOLD Screw,NewDeal HALLU Lock Plate System,NewDeal
Integra Lifesciences Corporation
K140283
02/04/2014
OSTEOMED EXTREMIFUSE SYSTEM
OSTEOMED
K190588
03/07/2019
Integra TITAN Reverse Shoulder System
Integra LifeSciences Corporation
K151021
04/16/2015
OsteoMed Cannulated Screw System
OSTEOMED CORP.
K131445
05/20/2013
OSTEOMED EXTREMILOCK FOOT PLATING SYSTEM
OSTEOMED LP
K181639
06/21/2018
Panta 2 Arthrodesis Nail System
Integra Lifesciences Corporation
K181999
07/26/2018
Integra TITAN Reverse Shoulder System
Integra Lifesciences Corporation
K133437
11/07/2013
1ST MTP PLATE
OSTEOMED
K133691
12/02/2013
EXTRIMILOCK ANKLE PLATING SYSTEM
OSTEOMED LP
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