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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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