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FDA 510(k) Applications Submitted by Genesis Fracture Care, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K160633
03/07/2016
G3(TM) Active Plate(R) Small Fragment System
GENESIS FRACTURE CARE, INC.
K171293
05/02/2017
G3Ö Active Plate« Miniature System
Genesis Fracture Care, Inc.
K152242
08/10/2015
G3┐ Active Plate« Large Fragment System
GENESIS FRACTURE CARE, INC.
K142938
10/09/2014
G3 Active Plate Large Fragment System
GENESIS FRACTURE CARE, INC.
K150649
03/12/2015
G3 Active Plate Large Fragment System
GENESIS FRACTURE CARE, INC.
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