FDA 510(k)

Tontarra Punches and Rongeurs

N.º K: K260446 · 2026-09-15

Fecha de decisión2026-09-15

Código de productoHAE

Comité asesorNE

DecisiónSubstantially Equivalent

Resumen del dispositivo

Tontarra Punches and Rongeurs is the device name listed in this FDA 510(k) record. The listed applicant is Tontarra Medizintechnik GmbH. It received FDA 510(k) clearance on 2026-09-15 under 510(k) number K260446. The device is classified under product code HAE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Tontarra Punches and Rongeurs?

Tontarra Punches and Rongeurs is a medical device that received FDA 510(k) clearance on 2026-09-15. The listed applicant is Tontarra Medizintechnik GmbH. The 510(k) number is K260446.

When did Tontarra Punches and Rongeurs receive FDA 510(k) clearance?

Tontarra Punches and Rongeurs received FDA 510(k) clearance on 2026-09-15, under 510(k) number K260446.

Who is the listed applicant for Tontarra Punches and Rongeurs?

The FDA 510(k) record lists Tontarra Medizintechnik GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Tontarra Punches and Rongeurs?

The FDA product code for Tontarra Punches and Rongeurs is HAE.

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Fuente oficial

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