FDA 510(k) Application Details - K970950

Device Classification Name	Orthosis, Spondyloisthesis Spinal Fixation   More FDA Info for this Device
510(K) Number	K970950
Device Name	Orthosis, Spondyloisthesis Spinal Fixation
Applicant	ACROMED CORP. 3303 CARNEGIE AVE. CLEVELAND, OH 44115 US Other 510(k) Applications for this Company
Contact	MARY LEWIS Other 510(k) Applications for this Contact
Regulation Number	888.3070   More FDA Info for this Regulation Number
Classification Product Code	MNH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/14/1997
Decision Date	06/03/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review