FDA 510(k)

MuscleView 2.0

Número K: K251682 · 2025-09-09

RequerenteSpringbok, Inc. (Dba Springbok Analytics)

Data da decisão2025-09-09

Código do produtoLNH

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

MuscleView 2.0 is the device name listed in this FDA 510(k) record. The listed applicant is Springbok, Inc. (Dba Springbok Analytics). It received FDA 510(k) clearance on 2025-09-09 under 510(k) number K251682. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the MuscleView 2.0?

MuscleView 2.0 is a medical device that received FDA 510(k) clearance on 2025-09-09. The listed applicant is Springbok, Inc. (Dba Springbok Analytics). The 510(k) number is K251682.

When did MuscleView 2.0 receive FDA 510(k) clearance?

MuscleView 2.0 received FDA 510(k) clearance on 2025-09-09, under 510(k) number K251682.

Who is the listed applicant for MuscleView 2.0?

The FDA 510(k) record lists Springbok, Inc. (Dba Springbok Analytics) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MuscleView 2.0?

The FDA product code for MuscleView 2.0 is LNH.

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