FDA 510(k) Application Details - K131311

Device Classification Name	Plate, Fixation, Bone   More FDA Info for this Device
510(K) Number	K131311
Device Name	Plate, Fixation, Bone
Applicant	JEIL MEDICAL CORPORATION #702, KOLON SCIENCE VALLEY 2ND 811, GURO-DONG, GURO-GU SEOUL-CITY 152-050 KR Other 510(k) Applications for this Company
Contact	JI-EUN KIM Other 510(k) Applications for this Contact
Regulation Number	888.3030   More FDA Info for this Regulation Number
Classification Product Code	HRS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/07/2013
Decision Date	09/05/2013
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review