FDA 510(k) Application Details - K220554

Device Classification Name	Orthopedic Stereotaxic Instrument   More FDA Info for this Device
510(K) Number	K220554
Device Name	Orthopedic Stereotaxic Instrument
Applicant	Taiwan Main Orthopaedic Biotechnology Co., Ltd. 1F., No. 46, Keya Rd., Daya Dist. Taichung City 428 TW Other 510(k) Applications for this Company
Contact	Jacky Fan 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	02/28/2022
Decision Date	12/16/2022
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