Geistlich Bio-Oss®— 510(k) K240661

Substantially Equivalent

Geistlich Pharma AG

FDA 510(k) clearance K240661 for Geistlich Bio-Oss®, Substantially Equivalent on 2024-07-12. Applicant: Geistlich Pharma AG. Device class: 2.

Clearance details

Applicant
Geistlich Pharma AG
Product code
Code NPM
Device class
Class 2
Regulation
21 CFR 872.3930
Advisory panel
Dental
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Wolhusen, CH
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