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

EVERSTICK A&O

K Number: K051953 · Decision Mar 21, 2006
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
41
Applicant Total
9
Review Days
246

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Basic Information

Device Name
EVERSTICK A&O
K Number
K051953
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.5470
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stick Tech , Ltd.
Date Received
July 18, 2005
Decision Date
March 21, 2006
Product Code
DYW
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
DYW Bracket, Plastic, Orthodontic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DYW), ordered by most recent decision date.

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Other Clearances by Stick Tech , Ltd.

K Number Device Name
K031341 STICK FLOW
K030820 EVERSTICK POST
K030072 EVERSTICK PERIO
K021126 EVERSTICK ORTHO
K011788 EVERSTICK
K011799 EVERSTICKNET
K003334 STICK NET
K003333 STICK