FDA 510(k) Application Details - K093553

Device Classification Name	Monitor, Spine Curvature   More FDA Info for this Device
510(K) Number	K093553
Device Name	Monitor, Spine Curvature
Applicant	PERSEUS ALTHETICS,LLC 1425 K STREET, N.W. SUITE 1100 WASHINGTON, DC 20005 US Other 510(k) Applications for this Company
Contact	KEITH BARRITT Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LZW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/17/2009
Decision Date	08/13/2010
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