FDA 510(k) Application Details - K002371

Device Classification Name	Appliance, Fixation, Spinal Intervertebral Body   More FDA Info for this Device
510(K) Number	K002371
Device Name	Appliance, Fixation, Spinal Intervertebral Body
Applicant	SPINEOLOGY, INC. 1815 NORTHWESTERN AVE. STILLWATER, MN 55082 US Other 510(k) Applications for this Company
Contact	PAMELA SNYDER Other 510(k) Applications for this Contact
Regulation Number	888.3060   More FDA Info for this Regulation Number
Classification Product Code	KWQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/27/2000
Decision Date	09/15/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review