FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

Straumann PURE Ceramic Implant System

K Number: K180477 · Decision Jan 4, 2019
Classifications
1
FEI Numbers
333
Registration Numbers
333
Same Product Code
1516
Applicant Total
49
Review Days
316

Basic Information

Device Name
Straumann PURE Ceramic Implant System
K Number
K180477
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Institut Straumann AG
Date Received
February 22, 2018
Decision Date
January 4, 2019
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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