FDA 510(k) Application Details - K233595

Device Classification Name	Orthopedic Stereotaxic Instrument   More FDA Info for this Device
510(K) Number	K233595
Device Name	Orthopedic Stereotaxic Instrument
Applicant	Genesys Spine 1250 S. Capital of Texas Highway Building 3, Suite 600 Austin, TX 78746 US Other 510(k) Applications for this Company
Contact	Derek Southard 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	11/08/2023
Decision Date	03/29/2024
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