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FDA 510(k)

Wishbone HA

K-Number: K211551 · 2021-08-20

ApplicantWishbone SA
Decision Date2021-08-20
Product CodeNPM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Wishbone HA is a medical device manufactured by Wishbone SA. It received FDA 510(k) clearance on 2021-08-20 under approval number K211551. The device is classified under product code NPM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Wishbone HA?

Wishbone HA is a medical device that received FDA 510(k) clearance on 2021-08-20. It is manufactured by Wishbone SA. The 510(k) number is K211551.

When was Wishbone HA approved by the FDA?

Wishbone HA received FDA 510(k) clearance on 2021-08-20, under approval number K211551.

What company makes Wishbone HA?

Wishbone HA is manufactured by Wishbone SA.

What is the FDA product code for Wishbone HA?

The FDA product code for Wishbone HA is NPM.

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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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