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FDA 510(k)

ALLONUS Tech Prosthetics

K-Number: K241616 · 2024-12-17

ApplicantAllonus Tech Co., Ltd.
Decision Date2024-12-17
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ALLONUS Tech Prosthetics is a medical device manufactured by Allonus Tech Co., Ltd.. It received FDA 510(k) clearance on 2024-12-17 under approval number K241616. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALLONUS Tech Prosthetics?

ALLONUS Tech Prosthetics is a medical device that received FDA 510(k) clearance on 2024-12-17. It is manufactured by Allonus Tech Co., Ltd.. The 510(k) number is K241616.

When was ALLONUS Tech Prosthetics approved by the FDA?

ALLONUS Tech Prosthetics received FDA 510(k) clearance on 2024-12-17, under approval number K241616.

What company makes ALLONUS Tech Prosthetics?

ALLONUS Tech Prosthetics is manufactured by Allonus Tech Co., Ltd..

What is the FDA product code for ALLONUS Tech Prosthetics?

The FDA product code for ALLONUS Tech Prosthetics is NHA.

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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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