FDA 510(k) Applications Submitted by STEPHEN 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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