FDA 510(k) Application Details - K200987

Device Classification Name	Screw, Fixation, Bone   More FDA Info for this Device
510(K) Number	K200987
Device Name	Screw, Fixation, Bone
Applicant	AzurMeds inc. 4809 N Ravenswood Avenue Suite 119 Chicago, IL 60604 US Other 510(k) Applications for this Company
Contact	Jean-Marie Berger Other 510(k) Applications for this Contact
Regulation Number	888.3040   More FDA Info for this Regulation Number
Classification Product Code	HWC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/15/2020
Decision Date	09/22/2020
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