FDA 510(k) Applications Submitted by JOHN SPAMPINATO

FDA 510(k) Number Submission Date Device Name Applicant
K030037 01/06/2003 UNIVERSAL TOTAL WRIST SYSTEM KINETIKOS MEDICAL, INC.
K023770 11/12/2002 K2 HEMI TOE IMPLANT SYSTEM (FORMERLY ZOBEL GREAT TOE IMPLANT SYSTEM) KINETIKOS MEDICAL, INC.
K040356 02/13/2004 KOMPRESSOR SCREW SYSTEM KINETIKOS MEDICAL, INC.
K061465 05/26/2006 KMI CEMENT RESTRICTOR IMPLANT KINETIKOS MEDICAL, INC.
K041461 06/02/2004 KMI DISTAL VOLAR RADIUS PLATE SYSTEM KINETIKOS MEDICAL, INC.
K051611 06/17/2005 MBARESORB IMPLANT KINETIKOS MEDICAL, INC.
K032806 09/09/2003 KATALYST RADIAL HEAD IMPLANT KINETIKOS MEDICAL, INC.
K024233 12/23/2002 KOMPRESSOR SCREW SYSTEM KINETIKOS MEDICAL, INC.


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