Surgicraft , Ltd. is one of 25971 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgicraft , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (AC) DEVICE, SURGICRAFT SURGICAL MESH SYSTEM, SURGICRAFT SCREW FIXATION SYSTEM
10
Total
10
Cleared
0
Denied
Surgicraft , Ltd. has 10 FDA 510(k) cleared orthopedic devices. Based in Chicago, US.
Historical record: 10 cleared submissions from 1997 to 2011.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Surgicraft , Ltd.
10 devices
Cleared
Feb 15, 2011
SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (AC) DEVICE
Orthopedic
662d
Cleared
Jul 24, 2008
SURGICRAFT SURGICAL MESH SYSTEM
General & Plastic Surgery
336d
Cleared
Jun 13, 2008
SURGICRAFT SCREW FIXATION SYSTEM
Orthopedic
115d
Cleared
Jun 04, 2008
STALIF TT INTERVERTEBRAL BODY FUSION SYSTEM
Orthopedic
215d
Cleared
Jan 25, 2008
STALIF (TM) C
Orthopedic
150d
Cleared
Jun 29, 2005
STALIF TT
Orthopedic
68d
Cleared
Sep 08, 2004
STALIF TT
Orthopedic
85d
Cleared
Nov 08, 1999
TITANIUM HARTSHILL SYSTEM
Orthopedic
178d
Cleared
Sep 25, 1998
THE BONE TIE
Orthopedic
52d
Cleared
Aug 07, 1997
RANSFORD CERVICAL FIXATION SYSTEM
Orthopedic
219d