FDA 510(k) Application Details - K081540

Device Classification Name	Monitor, Spine Curvature   More FDA Info for this Device
510(K) Number	K081540
Device Name	Monitor, Spine Curvature
Applicant	PETER FISCHER CHRISTOPHSTR. 2 TUBINGEN D72072 DE Other 510(k) Applications for this Company
Contact	PETER FISCHER 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	06/02/2008
Decision Date	02/20/2009
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