FDA 510(k) Application Details - K233874

Device Classification Name	Plate, Bone   More FDA Info for this Device
510(K) Number	K233874
Device Name	Plate, Bone
Applicant	TechMah CMF 2099 Thunderhead Road, Suite 302 Knoxville, TN 37922 US Other 510(k) Applications for this Company
Contact	Mohamed Mahfouz Other 510(k) Applications for this Contact
Regulation Number	872.4760   More FDA Info for this Regulation Number
Classification Product Code	JEY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/07/2023
Decision Date	07/11/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review