INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE


Device Classification Name

intervertebral fusion device with bone graft, lumbar

510(k) Number K080673
Device Name INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE
Applicant
VERTEBRAL TECHNOLOGIES, INC.
14289 yellowpine
andover, 
MN 
55304

Applicant Contact philip b jarvi
Correspondent
VERTEBRAL TECHNOLOGIES, INC.
14289 yellowpine
andover, 
MN 
55304

Correspodent Contact philip b jarvi
Regulation Number 888.3080
Classification Product Code
MAX  
Date Received 03/10/2008
Decision Date 06/10/2008
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Orthopedic

510k Review Panel

Orthopedic

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No