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FDA 510(k) Applications Submitted by SURGICRAFT LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K072370
08/23/2007
SURGICRAFT SURGICAL MESH SYSTEM
SURGICRAFT LTD.
K080447
02/19/2008
SURGICRAFT SCREW FIXATION SYSTEM
SURGICRAFT LTD.
K091207
04/24/2009
SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (AC) DEVICE
SURGICRAFT LTD.
K072415
08/28/2007
STALIF (TM) C
SURGICRAFT LTD.
K073109
11/02/2007
STALIF TT INTERVERTEBRAL BODY FUSION SYSTEM
SURGICRAFT LTD.
K051027
04/22/2005
STALIF TT
SURGICRAFT LTD.
K041617
06/15/2004
STALIF TT
SURGICRAFT LTD.
K965221
12/31/1996
RANSFORD CERVICAL FIXATION SYSTEM
SURGICRAFT LTD.
K991662
05/14/1999
TITANIUM HARTSHILL SYSTEM
SURGICRAFT LTD.
K982719
08/04/1998
THE BONE TIE
SURGICRAFT LTD.
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