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 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.

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. 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.

Related Devices (Code: LNH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253808AIR Recon DLGE Medical Systems K261331I-Genius (100019400)Esaote, S.p.A.K260852MAGNETOM Flow.Elite;MAGNETOM Flow.Neo;MAGNETOM Flow.Rise;MAGNETOM Flow.PureSiemens Healthineers AG K260113uMR AstraShanghai United Imaging Healthcare Co., Ltd.K253862APERTO Lucent MRI SystemFujifilm Corporation K260746S-scan Open (100001800)Esaote, S.p.A.

Official Source

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