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FDA 510(k)

MuscleView

K-Number: K241331 · 2024-10-01

ApplicantSpringbok, Inc.
Decision Date2024-10-01
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MuscleView is a medical device manufactured by Springbok, Inc.. It received FDA 510(k) clearance on 2024-10-01 under approval number K241331. 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?

MuscleView is a medical device that received FDA 510(k) clearance on 2024-10-01. It is manufactured by Springbok, Inc.. The 510(k) number is K241331.

When was MuscleView approved by the FDA?

MuscleView received FDA 510(k) clearance on 2024-10-01, under approval number K241331.

What company makes MuscleView?

MuscleView is manufactured by Springbok, Inc..

What is the FDA product code for MuscleView?

The FDA product code for MuscleView 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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