FDA 510(k) Application Details - K230276

Device Classification Name	Driver, Wire, And Bone Drill, Manual   More FDA Info for this Device
510(K) Number	K230276
Device Name	Driver, Wire, And Bone Drill, Manual
Applicant	TECHFIT Digital Surgery 1511 Aviation Center Pkwy Suite 220H Daytona Beach, FL 32114 US Other 510(k) Applications for this Company
Contact	Angela Marφa Lema-PΘrez Other 510(k) Applications for this Contact
Regulation Number	872.4120   More FDA Info for this Regulation Number
Classification Product Code	DZJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/01/2023
Decision Date	06/23/2023
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