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Centerpulse Spine-Tech, Inc.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K033679 COPSIOS BONE VOID FILLER (BVF)MQV2004-07-07 View
510(k) K031511 DYNESYS SPINAL SYSTEMNQP2004-03-05 View
510(k) K022615 CENTERPULSE, SPINE-TECH DIVISION CEMENT RESTRICTORJDK2002-10-29 View
510(k) K022344 TRINICA SELECT ANTERIOR CERVICAL PLATE SYSTEMKWQ2002-09-24 View
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