FDA 510(k)

Ball Joint Guide Array (66295)

Número K: K250893 · 2025-09-04

Data da decisão2025-09-04

Código do produtoHAW

Comité consultivoNE

DecisãoSubstantially Equivalent

Resumo do dispositivo

Ball Joint Guide Array (66295) is the device name listed in this FDA 510(k) record. The listed applicant is Bayer Medical Care, Inc.. It received FDA 510(k) clearance on 2025-09-04 under 510(k) number K250893. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Ball Joint Guide Array (66295)?

Ball Joint Guide Array (66295) is a medical device that received FDA 510(k) clearance on 2025-09-04. The listed applicant is Bayer Medical Care, Inc.. The 510(k) number is K250893.

When did Ball Joint Guide Array (66295) receive FDA 510(k) clearance?

Ball Joint Guide Array (66295) received FDA 510(k) clearance on 2025-09-04, under 510(k) number K250893.

Who is the listed applicant for Ball Joint Guide Array (66295)?

The FDA 510(k) record lists Bayer Medical Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ball Joint Guide Array (66295)?

The FDA product code for Ball Joint Guide Array (66295) is HAW.

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Fonte oficial

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