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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