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FDA 510(k) Applications Submitted by DAVE STINSON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K020562
02/20/2002
APEX INTRAMEDULLARY NAIL SYSTEM
MAGLY ORTHOPEDICS, LLC
K021579
05/14/2002
MAGLY 4.0 AND 5.5 MM LOCKING SYSTEM
MAGLY ORTHOPEDICS, LLC
K021662
05/20/2002
MAGLY 6.5MM CANNULATED SCREWS
MAGLY ORTHOPEDICS, LLC
K963937
10/01/1996
NORTHWEST PRECISION TECHNOLOGIES 6.5 MM CANNULATED CANNULATED CANCELLOUS SCREW
NORTHWEST PRECISION TECHNOLOGIES
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