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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 a medical device manufactured by Momentum Health, Inc.. It received FDA 510(k) clearance on 2023-10-04 under approval 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. It is manufactured by Momentum Health, Inc.. The 510(k) number is K232023.

When was Momentum Spine approved by the FDA?

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

What company makes Momentum Spine?

Momentum Spine is manufactured by Momentum Health, Inc..

What is the FDA product code for Momentum Spine?

The FDA product code for Momentum Spine is LDK.

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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.

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