FDA 510(k) Application Details - K032520

Device Classification Name	Plate, Bone   More FDA Info for this Device
510(K) Number	K032520
Device Name	Plate, Bone
Applicant	TEKKA 6512 BANNOCKBURN DRIVE BETHESDA, MD 20817 US Other 510(k) Applications for this Company
Contact	FAYYAZ MEMON Other 510(k) Applications for this Contact
Regulation Number	872.4760   More FDA Info for this Regulation Number
Classification Product Code	JEY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/15/2003
Decision Date	11/12/2003
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