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FDA 510(k) Applications Submitted by BRUCE HOOPER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K160924
04/04/2016
Amendia Interbody Fusion Devices
AMENDIA, INC.
K150395
02/18/2015
Omega LIF System
AMENDIA, INC.
K151310
05/18/2015
Amendia Interbody Fusion Devices
AMENDIA, INC.
K151322
05/18/2015
Amendia Interbody Fusion Devices
AMENDIA, INC.
K161842
07/05/2016
Overwatch Spine System
Amendia, Inc.
K152460
08/28/2015
Rectangular Corpectomy Cage
Amendia, Inc.
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