Surgicraft , Ltd.
Surgicraft , Ltd. holds FDA 510(k) medical device clearances, first cleared 1997, most recent 2011.
Top product codes for Surgicraft , Ltd.
Recent clearances by Surgicraft , Ltd.
- K091207 — SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (AC) DEVICE
- K072370 — SURGICRAFT SURGICAL MESH SYSTEM
- K080447 — SURGICRAFT SCREW FIXATION SYSTEM
- K073109 — STALIF TT INTERVERTEBRAL BODY FUSION SYSTEM
- K072415 — STALIF (TM) C
- K051027 — STALIF TT
- K041617 — STALIF TT
- K991662 — TITANIUM HARTSHILL SYSTEM
- K982719 — THE BONE TIE
- K965221 — RANSFORD CERVICAL FIXATION SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.