FDA 510(k) Application Details - K120680

Device Classification Name	Arthroscope   More FDA Info for this Device
510(K) Number	K120680
Device Name	Arthroscope
Applicant	SPINE VIEW, INC. 48810 Kato Rd. Suite 100E Fremont, CA 94538 US Other 510(k) Applications for this Company
Contact	Diana DeGregorio Other 510(k) Applications for this Contact
Regulation Number	888.1100   More FDA Info for this Regulation Number
Classification Product Code	HRX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/06/2012
Decision Date	06/26/2012
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review