FDA 510(k) Application Details - K242009

Device Classification Name	Orthopedic Stereotaxic Instrument   More FDA Info for this Device
510(K) Number	K242009
Device Name	Orthopedic Stereotaxic Instrument
Applicant	Kico Knee Innovation Company Pty Ltd Unit 1, 25 Frenchs Forest Rd E French Forest 2086 AU Other 510(k) Applications for this Company
Contact	Danyon Munro 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	07/10/2024
Decision Date	08/08/2024
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