FDA 510(k) Application Details - K113273

Device Classification Name	Retractor, Self-Retaining, For Neurosurgery   More FDA Info for this Device
510(K) Number	K113273
Device Name	Retractor, Self-Retaining, For Neurosurgery
Applicant	JOHNSON & JOHNSON 325 Paramount Drive Raynham, MA 02767 US Other 510(k) Applications for this Company
Contact	LAURA BLEYENDAAL Other 510(k) Applications for this Contact
Regulation Number	882.4800   More FDA Info for this Regulation Number
Classification Product Code	GZT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/07/2011
Decision Date	01/27/2012
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