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FDA 510(k) Applications Submitted by ETHEL BERNAL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K080526
02/26/2008
SIERRA SYSTEM
SEASPINE, INC.
K071726
06/25/2007
ZUMA
SEASPINE, INC.
K092521
08/18/2009
ZUMA-C
SEASPINE, INC.
K122571
08/23/2012
MALIBU SPINAL SYSTEM WITH THE DAYTONA DEFORMITY SYSTEM
SEASPINE, INC.
K072605
09/17/2007
MALIBU SPINAL SYSTEM
SEASPINE, INC.
K072729
09/26/2007
SIERRA
SEASPINE, INC.
K083089
10/16/2008
NEWPORT SPINAL SYSTEM
SEASPINE, INC.
K103297
11/08/2010
REDONDO-L
SEASPINE, INC.
K083338
11/12/2008
CARDIFF ANTERIOR CERVICAL PLATE SYSTEM
SEASPINE, INC.
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