FDA 510(k) Applications Submitted by GREG CANNEDY

FDA 510(k) Number Submission Date Device Name Applicant
K020069 01/09/2002 MEDTRONIC MIDA REX LEGEND SYSTEM, MIDAS REX LEGEND PNEUMATIC HIGH SPEED SYSTEM OR LEGEND SYSTEM MEDTRONIC MIDAS REX
K972718 07/21/1997 M-2 ANTERIOR PLATE SYSTEM ACROMED CORP.
K974757 12/19/1997 KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS ACROMED CORP.
K953978 08/23/1995 ANTERIOR DYNAMIZED SYSTEM ACROMED CORP.


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