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FDA 510(k)

EffortMed Spinal Fixation System

K-Number: K243946 · 2025-01-15

Decision Date2025-01-15
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EffortMed Spinal Fixation System is a medical device manufactured by Effortmed, LLC. It received FDA 510(k) clearance on 2025-01-15 under approval number K243946. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EffortMed Spinal Fixation System?

EffortMed Spinal Fixation System is a medical device that received FDA 510(k) clearance on 2025-01-15. It is manufactured by Effortmed, LLC. The 510(k) number is K243946.

When was EffortMed Spinal Fixation System approved by the FDA?

EffortMed Spinal Fixation System received FDA 510(k) clearance on 2025-01-15, under approval number K243946.

What company makes EffortMed Spinal Fixation System?

EffortMed Spinal Fixation System is manufactured by Effortmed, LLC.

What is the FDA product code for EffortMed Spinal Fixation System?

The FDA product code for EffortMed Spinal Fixation System is NKB.

Related Clinical Trials

Related PubMed Literature

Other Devices by Effortmed, LLC

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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.