FDA 510(k) Application Details - K170243

Device Classification Name	Intervertebral Fusion Device With Bone Graft, Lumbar   More FDA Info for this Device
510(K) Number	K170243
Device Name	Intervertebral Fusion Device With Bone Graft, Lumbar
Applicant	CORENTEC CO., LTD 12, YEONGSANHONG 1-GIL, IPJANG-MYEON, SEOBUK GU Cheonan-si 31056 KR Other 510(k) Applications for this Company
Contact	J.S. DANIEL Other 510(k) Applications for this Contact
Regulation Number	888.3080   More FDA Info for this Regulation Number
Classification Product Code	MAX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/26/2017
Decision Date	03/31/2017
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review