Medical Device Manufacturer · US , Chicago , IL

Surgicraft , Ltd. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1997
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
1-10 of 10
Cleared Feb 15, 2011
SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (AC) DEVICE
K091207 · HTN
Orthopedic · 662d
Cleared Jul 24, 2008
SURGICRAFT SURGICAL MESH SYSTEM
K072370 · FTL
General & Plastic Surgery · 336d
Cleared Jun 13, 2008
SURGICRAFT SCREW FIXATION SYSTEM
K080447 · MBI
Orthopedic · 115d
Cleared Jun 04, 2008
STALIF TT INTERVERTEBRAL BODY FUSION SYSTEM
K073109 · OVD
Orthopedic · 215d
Cleared Jan 25, 2008
STALIF (TM) C
K072415 · OVE
Orthopedic · 150d
Cleared Jun 29, 2005
STALIF TT
K051027 · MQP
Orthopedic · 68d
Cleared Sep 08, 2004
STALIF TT
K041617 · MQP
Orthopedic · 85d
Cleared Nov 08, 1999
TITANIUM HARTSHILL SYSTEM
K991662 · KWP
Orthopedic · 178d
Cleared Sep 25, 1998
THE BONE TIE
K982719 · HTY
Orthopedic · 52d
Cleared Aug 07, 1997
RANSFORD CERVICAL FIXATION SYSTEM
K965221 · KWP
Orthopedic · 219d
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All10 Orthopedic 9 General & Plastic Surgery 1