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FDA 510(k) Applications Submitted by NICOLE BOWDEN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K071879
07/09/2007
ZIMMER DTO IMPLANT
ZIMMER SPINE, INC
K071880
07/09/2007
Optima ZS Transition Screw
ZIMMER SPINE, INC
K102721
09/21/2010
LIVEWIRE ELECTOPHYSIOLOGY CATHETER
ST. JUDE MEDICAL
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