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

FRIADENT CERCON AND ANKYLOS CERCON BALANCE ABUTMENTS

K Number: K072730 · Decision Mar 27, 2008
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
279
Review Days
183

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Basic Information

Device Name
FRIADENT CERCON AND ANKYLOS CERCON BALANCE ABUTMENTS
K Number
K072730
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentsply Intl.
Date Received
September 26, 2007
Decision Date
March 27, 2008
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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