This page includes the latest FDA filings for Surgicraft L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Device Company | Device | Date |
---|---|---|
SURGICRAFT LTD. | SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (AC) DEVICE | 2011-02-15 |
SURGICRAFT LTD. | SURGICRAFT SURGICAL MESH SYSTEM | 2008-07-24 |
SURGICRAFT LTD. | SURGICRAFT SCREW FIXATION SYSTEM | 2008-06-13 |
SURGICRAFT LTD. | STALIF TT INTERVERTEBRAL BODY FUSION SYSTEM | 2008-06-04 |
SURGICRAFT LTD. | STALIF (TM) C | 2008-01-25 |
SURGICRAFT LTD. | STALIF TT | 2005-06-29 |
SURGICRAFT LTD. | STALIF TT | 2004-09-08 |
SURGICRAFT LTD. | TITANIUM HARTSHILL SYSTEM | 1999-11-08 |
SURGICRAFT LTD. | THE BONE TIE | 1998-09-25 |
SURGICRAFT LTD. | RANSFORD CERVICAL FIXATION SYSTEM | 1997-08-07 |
NCAGE Code | 0L133 | SURGICRAFT LTD |
NCAGE Code | U8698 | SURGICRAFT LTD |
CAGE Code | 0L133 | SURGICRAFT LTD |
CAGE Code | U8698 | SURGICRAFT LTD |