FDA 510(k) Application Details - K201793

Device Classification Name	Intervertebral Fusion Device With Bone Graft, Cervical   More FDA Info for this Device
510(K) Number	K201793
Device Name	Intervertebral Fusion Device With Bone Graft, Cervical
Applicant	JMT Co., Ltd 70-39, Gwonyul-ro 1203 beon-gile, Baekseok-eup Yangju-si 11517 KR Other 510(k) Applications for this Company
Contact	Sang-Ok Nam Other 510(k) Applications for this Contact
Regulation Number	888.3080   More FDA Info for this Regulation Number
Classification Product Code	ODP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/30/2020
Decision Date	09/13/2021
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