FDA 510(k) Application Details - K981881

Device Classification Name	Screw, Fixation, Intraosseous   More FDA Info for this Device
510(K) Number	K981881
Device Name	Screw, Fixation, Intraosseous
Applicant	DOCTOR'S RESEARCH GROUP, INC. 143 WOLCOTT RD. WOLCOTT, CT 06716 US Other 510(k) Applications for this Company
Contact	RICHARD DESLAURIERS Other 510(k) Applications for this Contact
Regulation Number	872.4880   More FDA Info for this Regulation Number
Classification Product Code	DZL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/28/1998
Decision Date	12/02/1998
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