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FDA 510(k)

Momentum Spine

K-Number: K232023 · 2023-10-04

ApplicantMomentum Health, Inc.
Decision Date2023-10-04
Product CodeLDK
DecisionSubstantially Equivalent

Device Summary

Momentum Spine is the device name listed in this FDA 510(k) record. The listed applicant is Momentum Health, Inc.. It received FDA 510(k) clearance on 2023-10-04 under 510(k) number K232023. The device is classified under product code LDK. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Momentum Spine?

Momentum Spine is a medical device that received FDA 510(k) clearance on 2023-10-04. The listed applicant is Momentum Health, Inc.. The 510(k) number is K232023.

When did Momentum Spine receive FDA 510(k) clearance?

Momentum Spine received FDA 510(k) clearance on 2023-10-04, under 510(k) number K232023.

Who is the listed applicant for Momentum Spine?

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

What is the FDA product code for Momentum Spine?

The FDA product code for Momentum Spine is LDK.

Related Devices (Code: LDK)

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.

K230463NSite Scoliosis Assessment AppNsite, Inc.K183485CryoVizion SystemCryos Technologies, Inc.

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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