FDA 510(k) Application Details - K023462

Device Classification Name	Manipulator, Plunger-Like Joint   More FDA Info for this Device
510(K) Number	K023462
Device Name	Manipulator, Plunger-Like Joint
Applicant	NEUROMECHANICAL INNOVATIONS, LLC 11011 S. 48TH ST. SUITE 205 PHOENIX, AZ 85044 US Other 510(k) Applications for this Company
Contact	CHRISTOPHER J COLLOCA Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LXM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/15/2002
Decision Date	01/13/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review