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

ANGLED XIVE MP ABUTMENT, ANGLED ANKYLOS

K Number: K122268 · Decision Dec 11, 2012
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
23
Review Days
134

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Basic Information

Device Name
ANGLED XIVE MP ABUTMENT, ANGLED ANKYLOS
K Number
K122268
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentsply International
Date Received
July 30, 2012
Decision Date
December 11, 2012
Product Code
NHA
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
NHA Abutment, Implant, Dental, Endosseous

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