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

ANKYLOS C/X IMPLANT SYSTEM

K Number: K140347 · Decision Aug 20, 2014
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
12
Review Days
190

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Basic Information

Device Name
ANKYLOS C/X IMPLANT SYSTEM
K Number
K140347
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentsply Intl., Inc.
Date Received
February 11, 2014
Decision Date
August 20, 2014
Product Code
DZE
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
DZE Implant, Endosseous, Root-Form

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