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510(k) clearance

Tontarra Punches and Rongeurs

FDA 510(k) source

510(k) number
K260446
Applicant
Tontarra Medizintechnik GmbH
Decision date
Sep 15, 2026
Date received
Feb 11, 2026
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
HAE
Device type
Rongeur, Manual
Device class
Class II
Regulation
21 CFR 882.4840
Advisory committee
Neurology
Statement or summary
Summary
Third party
N
Location
Wurmlingen, DE