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FDA 510(k) Applications Submitted by STEPHEN M PALUMBO
FDA 510(k) Number
Submission Date
Device Name
Applicant
K053276
11/23/2005
IST PEDICLE SCREW SYSTEM
INNOVATIVE SPINAL TECHNOLOGIES INC
K012362
07/25/2001
MODIFICATION TO VASCULAR CLOSURE DEVICE
STD MFG., INC.
K003169
10/10/2000
VASCULAR CLOSURE DEVICE
STD MFG., INC.
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