FDA 510(k) Application Details - K213380

Device Classification Name	Orthopedic Stereotaxic Instrument   More FDA Info for this Device
510(K) Number	K213380
Device Name	Orthopedic Stereotaxic Instrument
Applicant	Kico Knee Innovation Company Pty Limited Suite 3, Building 1, 20 Bridge Street Pymble 2073 AU Other 510(k) Applications for this Company
Contact	Stefanie Auf Der Mauer 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	10/13/2021
Decision Date	01/11/2022
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