FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

PRE-CEMENTED ORTHODONTIC BRACKET SYSTEM EXTENSION II

K Number: K093221 · Decision Oct 30, 2009
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
192
Applicant Total
12
Review Days
17

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Basic Information

Device Name
PRE-CEMENTED ORTHODONTIC BRACKET SYSTEM EXTENSION II
K Number
K093221
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.3750
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentsply Intl., Inc.
Date Received
October 13, 2009
Decision Date
October 30, 2009
Product Code
DYH
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DYH Adhesive, Bracket And Tooth Conditioner, Resin

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