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FDA 510(k)

Bonelogic

K-Number: K223757 · 2023-12-08

ApplicantDisior, Ltd.
Decision Date2023-12-08
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Bonelogic is a medical device manufactured by Disior, Ltd.. It received FDA 510(k) clearance on 2023-12-08 under approval number K223757. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Bonelogic?

Bonelogic is a medical device that received FDA 510(k) clearance on 2023-12-08. It is manufactured by Disior, Ltd.. The 510(k) number is K223757.

When was Bonelogic approved by the FDA?

Bonelogic received FDA 510(k) clearance on 2023-12-08, under approval number K223757.

What company makes Bonelogic?

Bonelogic is manufactured by Disior, Ltd..

What is the FDA product code for Bonelogic?

The FDA product code for Bonelogic is QIH.

Other Devices by Disior, Ltd.

K203290Bonelogic K240736SMART Bun-Yo-Matic X-Ray K240642SMART Bun-Yo-Matic CT K250023SMART PCFD K253764ENOS Software Guided External Fixation System

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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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