FDA 510(k) Application Details - K071334

Device Classification Name	Neurological Stereotaxic Instrument   More FDA Info for this Device
510(K) Number	K071334
Device Name	Neurological Stereotaxic Instrument
Applicant	DEPUY ORTHOPAEDICS, INC. 700 ORTHOPAEDIC DRIVE WARSAW, IN 46581-0988 US Other 510(k) Applications for this Company
Contact	RHONDA MYER Other 510(k) Applications for this Contact
Regulation Number	882.4560   More FDA Info for this Regulation Number
Classification Product Code	HAW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/11/2007
Decision Date	07/02/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review