FDA 510(k)

Articulator Arthroscopic Bur

Número K: K252666 · 2025-11-21

RequerenteJoint Preservation Innovations, LLC

Data da decisão2025-11-21

Código do produtoHRX

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

Articulator Arthroscopic Bur is the device name listed in this FDA 510(k) record. The listed applicant is Joint Preservation Innovations, LLC. It received FDA 510(k) clearance on 2025-11-21 under 510(k) number K252666. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Articulator Arthroscopic Bur?

Articulator Arthroscopic Bur is a medical device that received FDA 510(k) clearance on 2025-11-21. The listed applicant is Joint Preservation Innovations, LLC. The 510(k) number is K252666.

When did Articulator Arthroscopic Bur receive FDA 510(k) clearance?

Articulator Arthroscopic Bur received FDA 510(k) clearance on 2025-11-21, under 510(k) number K252666.

Who is the listed applicant for Articulator Arthroscopic Bur?

The FDA 510(k) record lists Joint Preservation Innovations, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Articulator Arthroscopic Bur?

The FDA product code for Articulator Arthroscopic Bur is HRX.

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