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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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