FDA 510(k) Application Details - K955503

Device Classification Name	Device, Jaw Repositioning   More FDA Info for this Device
510(K) Number	K955503
Device Name	Device, Jaw Repositioning
Applicant	JONATHAN A. PARKER, D.D.S. 1801 K STREET, N.W. WASHINGTON, DC 20006 US Other 510(k) Applications for this Company
Contact	ROBERT J STEFANI 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	12/01/1995
Decision Date	02/08/1996
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