STALIF (TM) C


Device Classification Name

intervertebral fusion device with bone graft, cervical

510(k) Number K072415
Device Name STALIF (TM) C
Applicant
SURGICRAFT LTD.
111 hill road
douglassville, 
PA 
19518

Applicant Contact donald w guthner
Correspondent
SURGICRAFT LTD.
111 hill road
douglassville, 
PA 
19518

Correspodent Contact donald w guthner
Regulation Number 888.3080
Classification Product Code
ODP  
Date Received 08/28/2007
Decision Date 01/25/2008
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Orthopedic

510k Review Panel

Orthopedic

summary

summary

Type Abbreviated
Reviewed by Third Party No

Combination Product

No