FDA 510(k) Application Details - K180796

Device Classification Name	Orthopedic Stereotaxic Instrument   More FDA Info for this Device
510(K) Number	K180796
Device Name	Orthopedic Stereotaxic Instrument
Applicant	Spineology Inc. 7800 3rd Street N., Suite 600 St. Paul, MN 55128 US Other 510(k) Applications for this Company
Contact	Jacqueline A. Hauge 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	03/27/2018
Decision Date	05/02/2018
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