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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name aligner, sequential
510(k) Number K193130
Device Name MVP Aligner System
Applicant
MVP Aligners, LLC
5-9 Union Square West
new york,  NY  10003
Applicant Contact daniel michaeli
Correspondent
REGULATORY TECHNOLOGY SERVICES, LLC
1000 Westgate Drive,
Suite 510k
saint paul,  MN  55114
Correspondent Contact prithul bom
Regulation Number872.5470
Classification Product Code
NXC  
Date Received11/12/2019
Decision Date 08/07/2020
Decision substantially equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
summary summary
Type Traditional
Reviewed by Third Party Yes
Combination Product No
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