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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Bracket, Metal, Orthodontic
510(k) Number K881233
Device Name STRAIGHT LENGTH ARCH WIRES
Applicant
Flexmedics
620 Ford Ctr., 420 N. Fifth
St.
Minneapolis,  MN  55401
Applicant Contact SIEVERT, JR.
Correspondent
Flexmedics
620 Ford Ctr., 420 N. Fifth
St.
Minneapolis,  MN  55401
Correspondent Contact SIEVERT, JR.
Regulation Number872.5410
Classification Product Code
EJF  
Date Received03/22/1988
Decision Date 04/12/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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