FDA 510(k) Application Details - K221180

Device Classification Name	Orthopedic Stereotaxic Instrument   More FDA Info for this Device
510(K) Number	K221180
Device Name	Orthopedic Stereotaxic Instrument
Applicant	Medtronic Sofamor Danek USA, INC 1800 Pyramid Place Memphis, TN 38132 US Other 510(k) Applications for this Company
Contact	Elizabeth Hamilton Other 510(k) Applications for this Contact
Regulation Number	882.4560   More FDA Info for this Regulation Number
Classification Product Code	OLO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/25/2022
Decision Date	05/25/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review