FDA 510(k) Application Details - K032410

Device Classification Name	Device, Jaw Repositioning   More FDA Info for this Device
510(K) Number	K032410
Device Name	Device, Jaw Repositioning
Applicant	JAMES P BOYD 710 MIDORI CT SOLANA BEACH, CA 92075 US Other 510(k) Applications for this Company
Contact	JAMES P BOYD Other 510(k) Applications for this Contact
Regulation Number	872.5570   More FDA Info for this Regulation Number
Classification Product Code	LQZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/04/2003
Decision Date	02/28/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review