Tontarra Punches and Rongeurs— 510(k) K260446

Name: FDA 510(k) clearance K260446
Creator: U.S. Food and Drug Administration
Published: 2026-09-15

Substantially Equivalent

Tontarra Medizintechnik GmbH

FDA 510(k) clearance K260446 for Tontarra Punches and Rongeurs, Substantially Equivalent on 2026-09-15. Applicant: Tontarra Medizintechnik GmbH. Device class: 2.

Clearance details

Applicant: Tontarra Medizintechnik GmbH
Product code: Code HAE
Device class: Class 2
Regulation: 21 CFR 882.4840
Advisory panel: Neurology
Date received: 2026-02-11
Decision date: 2026-09-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wurmlingen, DE

Download summary PDF View on FDA.gov ↗

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