FDA 510(k) Application Details - K143730

Device Classification Name	Plate, Bone   More FDA Info for this Device
510(K) Number	K143730
Device Name	Plate, Bone
Applicant	JEIL MEDICAL CORPORATION 702-706, 804, 805,807,812-HO ,55, DIGITAL-RO 34-GIL, GURO-GU SEOUL 152-728 KR Other 510(k) Applications for this Company
Contact	HYEROUNG LEE 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	12/29/2014
Decision Date	06/10/2015
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