STRAUMANN TIBRUSH— 510(k) K111724

Substantially Equivalent

Straumann USA

FDA 510(k) clearance K111724 for STRAUMANN TIBRUSH, Substantially Equivalent on 2011-09-12. Applicant: Straumann USA. Device class: 2.

Clearance details

Applicant: Straumann USA
Product code: Code ELB
Device class: Class 2
Regulation: 21 CFR 872.4840
Advisory panel: Dental
Date received: 2011-06-20
Decision date: 2011-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Andover, MA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.