FDA 510(k) Application Details - K210298

Device Classification Name	Resin, Denture, Relining, Repairing, Rebasing   More FDA Info for this Device
510(K) Number	K210298
Device Name	Resin, Denture, Relining, Repairing, Rebasing
Applicant	Pro3dure Medical GmbH Am Burgberg 13 Iserlohn 58642 DE Other 510(k) Applications for this Company
Contact	Frank Gischer Other 510(k) Applications for this Contact
Regulation Number	872.3760   More FDA Info for this Regulation Number
Classification Product Code	EBI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/03/2021
Decision Date	05/05/2021
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