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

FDA 510(k) Regulatory Record - Surgicraft , Ltd. Orthopedic ✕

9 devices

1-9 of 9

Cleared Feb 15, 2011

SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (AC) DEVICE

Orthopedic · 662d

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

Orthopedic · 150d

Cleared Jun 29, 2005

Orthopedic · 68d

Cleared Sep 08, 2004

Orthopedic · 85d

Cleared Nov 08, 1999

TITANIUM HARTSHILL SYSTEM

Orthopedic · 178d

Cleared Sep 25, 1998

Orthopedic · 52d

Cleared Aug 07, 1997

RANSFORD CERVICAL FIXATION SYSTEM

Orthopedic · 219d