FDA 510(k) Applications Submitted by CENTERPULSE SPINE-TECH, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K031511 05/14/2003 DYNESYS SPINAL SYSTEM CENTERPULSE SPINE-TECH, INC.
K022615 08/07/2002 CENTERPULSE, SPINE-TECH DIVISION CEMENT RESTRICTOR CENTERPULSE SPINE-TECH, INC.
K022344 07/19/2002 TRINICA SELECT ANTERIOR CERVICAL PLATE SYSTEM CENTERPULSE SPINE-TECH, INC.
K033679 11/24/2003 COPSIOS BONE VOID FILLER (BVF) CENTERPULSE SPINE-TECH, INC.


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