FDA 510(k) Application Details - K241073

Device Classification Name	Intervertebral Fusion Device With Bone Graft, Lumbar   More FDA Info for this Device
510(K) Number	K241073
Device Name	Intervertebral Fusion Device With Bone Graft, Lumbar
Applicant	Shenzhen Dazhou Medical Technology Co., Ltd. Suite B605, Building No.1, Yesun Intelligent Community ll, 1301-76 Guanguang Rd., Longhua District Shenzhen 518110 CN Other 510(k) Applications for this Company
Contact	Jingzhou Yang 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	04/19/2024
Decision Date	12/06/2024
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