FDA 510(k) Application Details - K241412

Device Classification Name	Aligner, Sequential   More FDA Info for this Device
510(K) Number	K241412
Device Name	Aligner, Sequential
Applicant	Align Technology, Inc. 2820 Orchard Parkway San Jose, CA 95134 US Other 510(k) Applications for this Company
Contact	Nestor Vazquez Salgado Other 510(k) Applications for this Contact
Regulation Number	872.5470   More FDA Info for this Regulation Number
Classification Product Code	NXC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/17/2024
Decision Date	06/18/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review