FDA 510(k) Applications Submitted by KIM THURMAN

FDA 510(k) Number Submission Date Device Name Applicant
K012254 07/18/2001 VBR OSTEOTECH, INC.
K003155 10/10/2000 VERTEBRAL BODY REPLACEMENT OSTEOTECH, INC.
K003384 10/31/2000 VERSALINK TITANIUM ROD-TO-ROD COUPLERS OSTEOTECH, INC.


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