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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