FDA 510(k) Application Details - K083310

Device Classification Name	Orthopedic Stereotaxic Instrument   More FDA Info for this Device
510(K) Number	K083310
Device Name	Orthopedic Stereotaxic Instrument
Applicant	BRAINLAB AG KAPELLENSTRASSE 12 FELDKIRCHEN 85622 DE Other 510(k) Applications for this Company
Contact	RAINER BIRKENBACH Other 510(k) Applications for this Contact
Regulation Number	882.4560   More FDA Info for this Regulation Number
Classification Product Code	OLO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/10/2008
Decision Date	04/01/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review