FDA 510(k) Application Details - K093711

Device Classification Name	Cord, Retraction   More FDA Info for this Device
510(K) Number	K093711
Device Name	Cord, Retraction
Applicant	SEPTODONT 1050 CONNECTICUT AVE., NW WASHINGTON, DC 20036 US Other 510(k) Applications for this Company
Contact	WAYNE MATELSKI, ESQ Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	MVL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/01/2009
Decision Date	02/17/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review