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FDA 510(k) Applications Submitted by BRIAN HOCKETT
FDA 510(k) Number
Submission Date
Device Name
Applicant
K130832
03/26/2013
ORTHOHELIX STAPLE SYSTEM
ORTHOHELIX SURGICAL DESIGNS, INC.
K150871
04/01/2015
ForeFoot STP System
TORNIER, INC.
K141004
04/18/2014
INTRAOSSEOUS FIXATION SYSTEM
ORTHOHELIX SURGICAL DESIGNS, INC.
K131324
05/08/2013
MAXTORQUE SCREW SYSTEM
ORTHOHELIX SURGICAL DESIGNS, INC.
K141301
05/19/2014
MAXLOCK EXTREME ELBOW FRACTURE SYSTEM
ORTHOHELIX SURGICAL DESIGNS, INC.
K142148
08/05/2014
ORTHOHELIX STAPLE SYSTEM
ORTHOHELIX SURGICAL DESIGNS, INC.
K132733
09/03/2013
ORTHOHELIX SYNDESMOSIS FIXATION DEVICES
ORTHOHELIX SURGICAL DESIGNS, INC.
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