FDA 510(k) Applications Submitted by David Hooper

FDA 510(k) Number Submission Date Device Name Applicant
K210266 02/01/2021 OverStitch Sx Endoscopic Suturing System Apollo Endosurgery Inc.
K142141 08/05/2014 STARBAND, STARLIGHT ORTHOMERICA PRODUCTS, INC.
K140353 02/12/2014 STARBAND AND STARLIGHT ORTHOMERICA PRODUCTS, INC.
K133250 10/22/2013 STARLIGHT ORTHOMERICA PRODUCTS, INC.
K124023 12/28/2012 STARBAND ORTHOMERICA PRODUCTS, INC.
K020611 02/25/2002 UNIVERSAL BONE PLATE III SYSTEM (UBP III) SPINAL CONCEPTS, INC.
K010563 02/26/2001 END-TO-END AND SIDE-BY-SIDE CONNECTORS SPINAL CONCEPTS, INC.
K021009 03/28/2002 OCTAFIX OCCIPITAL CERVICAL PLATING SYSTEM SPINAL CONCEPTS, INC.
K021564 05/13/2002 INCOMPASS SPINAL FIXATION SYSTEM SPINAL CONCEPTS, INC.
K021719 05/23/2002 FORTITUDE CEMENT RESTRICTOR SPINAL CONCEPTS, INC.
K022218 07/09/2002 CADENCE CEMENT RESTRICTOR SPINAL CONCEPTS, INC.
K002082 07/10/2000 SPEEDLINK TRANSVERSE CONNECTOR SPINAL CONCEPTS, INC.
K003351 10/26/2000 PARSFIX CABLE-SCREW SYSTEM SPINAL CONCEPTS, INC.
K013979 12/03/2001 SC-ACUFIX THINLINE ANTERIOR CERVICAL PLATE SYSTEM SPINAL CONCEPTS, INC.
DEN210045 09/30/2021 APOLLO ESG System, APOLLO ESG SX System, APOLLO REVISE System, APOLLO REVISE SX System Apollo Endosurgery, Inc.


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