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

Straumann BoneCeramic

K Number: K201051 · Decision Sep 24, 2020
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
229
Applicant Total
90
Review Days
156

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Basic Information

Device Name
Straumann BoneCeramic
K Number
K201051
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Institut Straumann AG
Date Received
April 21, 2020
Decision Date
September 24, 2020
Product Code
LYC
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
LYC Bone Grafting Material, Synthetic

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