FDA 510(k) Application Details - K193203

Device Classification Name	Intervertebral Fusion Device With Bone Graft, Lumbar   More FDA Info for this Device
510(K) Number	K193203
Device Name	Intervertebral Fusion Device With Bone Graft, Lumbar
Applicant	K2M, Inc. 600 Hope Parkway SE Leesburg, VA 21075 US Other 510(k) Applications for this Company
Contact	Oonagh Lahiff 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	11/20/2019
Decision Date	02/18/2020
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