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FDA 510(k)

MuscleView 2.0

K-Number: K251682 · 2025-09-09

ApplicantSpringbok, Inc. (Dba Springbok Analytics)
Decision Date2025-09-09
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

What is the MuscleView 2.0?

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

When was MuscleView 2.0 approved by the FDA?

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

What company makes MuscleView 2.0?

MuscleView 2.0 is manufactured by Springbok, Inc. (Dba Springbok Analytics).

What is the FDA product code for MuscleView 2.0?

The FDA product code for MuscleView 2.0 is LNH.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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