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FDA 510(k)

Neoss Individual Prosthetics

K-Number: K211396 · 2022-05-17

ApplicantNeoss, Ltd.
Decision Date2022-05-17
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Neoss Individual Prosthetics is a medical device manufactured by Neoss, Ltd.. It received FDA 510(k) clearance on 2022-05-17 under approval number K211396. 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 Neoss Individual Prosthetics?

Neoss Individual Prosthetics is a medical device that received FDA 510(k) clearance on 2022-05-17. It is manufactured by Neoss, Ltd.. The 510(k) number is K211396.

When was Neoss Individual Prosthetics approved by the FDA?

Neoss Individual Prosthetics received FDA 510(k) clearance on 2022-05-17, under approval number K211396.

What company makes Neoss Individual Prosthetics?

Neoss Individual Prosthetics is manufactured by Neoss, Ltd..

What is the FDA product code for Neoss Individual Prosthetics?

The FDA product code for Neoss Individual 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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