FDA 510(k) Application Details - K250879

Device Classification Name	Orthopedic Stereotaxic Instrument   More FDA Info for this Device
510(K) Number	K250879
Device Name	Orthopedic Stereotaxic Instrument
Applicant	Proprio, Inc. 111 W. John St., Suite 308 Seattle, WA 98119 US Other 510(k) Applications for this Company
Contact	Shannon Eubanks 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	03/24/2025
Decision Date	06/04/2025
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review