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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