FDA 510(k) FDA unclassified Substantially Equivalent 🇨🇭 Switzerland

Straumann PrefGel

K Number: K162311 · Decision Mar 7, 2017
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
40
Applicant Total
90
Review Days
201

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Basic Information

Device Name
Straumann PrefGel
K Number
K162311
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Institut Straumann AG
Date Received
August 18, 2016
Decision Date
March 7, 2017
Product Code
KJJ
Advisory Committee
Unknown
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
KJJ Cleanser, Root Canal

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K253315 Straumann Variobase Abutments XC for Bridge/Bar
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K243278 Custom Abutments
K243478 Straumann InLab Validated Workflow
K233252 Straumann CARES Visual and Nova Dental CAD
K241391 Straumann® PURE Ceramic Implants
K234049 Straumann® BLC and TLC Implants - Line extension
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