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Surgicraft , Ltd.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K091207 SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (AC) DEVICEHTN2011-02-15 View
510(k) K072370 SURGICRAFT SURGICAL MESH SYSTEMFTL2008-07-24 View
510(k) K080447 SURGICRAFT SCREW FIXATION SYSTEMMBI2008-06-13 View
510(k) K073109 STALIF TT INTERVERTEBRAL BODY FUSION SYSTEMOVD2008-06-04 View
510(k) K072415 STALIF (TM) COVE2008-01-25 View
510(k) K051027 STALIF TTMQP2005-06-29 View
510(k) K041617 STALIF TTMQP2004-09-08 View
510(k) K991662 TITANIUM HARTSHILL SYSTEMKWP1999-11-08 View
510(k) K982719 THE BONE TIEHTY1998-09-25 View
510(k) K965221 RANSFORD CERVICAL FIXATION SYSTEMKWP1997-08-07 View
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