FDA 510(k) Application Details - K030820

Device Classification Name	Post, Root Canal   More FDA Info for this Device
510(K) Number	K030820
Device Name	Post, Root Canal
Applicant	STICK TECH LTD. 80 PARKWAY WEST MOUNT VERNON, NY 10552 US Other 510(k) Applications for this Company
Contact	WILLIAM TROETEL Other 510(k) Applications for this Contact
Regulation Number	872.3810   More FDA Info for this Regulation Number
Classification Product Code	ELR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/14/2003
Decision Date	05/20/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review