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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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