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FDA 510(k) Applications Submitted by WENZEL SPINE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K120603
02/28/2012
VARILIFT -C
WENZEL SPINE
K100820
03/23/2010
WENZEL SPINE VARILIFT INTERBODY FUSION SYSTEM
WENZEL SPINE
K111123
04/21/2011
VARILIFT CERVICAL INTERBODY FUSION SYSTEM
WENZEL SPINE
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