FDA 510(k) Applications Submitted by JEFF BRITTAN

FDA 510(k) Number Submission Date Device Name Applicant
K130830 03/26/2013 INTEGRA LAMINOPLASTY SYSTEM SEASPINE, INC.
K082309 08/13/2008 CAMBRIA SEASPINE, INC.
K082310 08/13/2008 HOLLYWOOD, PACIFICA, REDONDO, VENTURA SEASPINE, INC.
K082926 10/01/2008 ZUMA, MODEL 55-XXXX/56-XXXX SEASPINE, INC.
K133418 11/07/2013 INTEGRA EXPANDABLE INTERVEREBRAL BODY FUSION DEVICE (IBD) SYSTEM SEASPINE, INC.


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