FDA 510(k) Application Details - K210159

Device Classification Name	Screw, Fixation, Bone   More FDA Info for this Device
510(K) Number	K210159
Device Name	Screw, Fixation, Bone
Applicant	Fusion Orthopedics, LLC 4135 S. Powder Rd., Suite 110 Mesa, AZ 85212 US Other 510(k) Applications for this Company
Contact	Whitney Rey 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	01/21/2021
Decision Date	07/23/2021
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