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FDA 510(k)

Acute QC Strut and Components

K-Number: K221792 · 2022-08-25

Decision Date2022-08-25
Product CodeOSN
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Acute QC Strut and Components is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2022-08-25 under 510(k) number K221792. The device is classified under product code OSN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Acute QC Strut and Components?

Acute QC Strut and Components is a medical device that received FDA 510(k) clearance on 2022-08-25. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K221792.

When did Acute QC Strut and Components receive FDA 510(k) clearance?

Acute QC Strut and Components received FDA 510(k) clearance on 2022-08-25, under 510(k) number K221792.

Who is the listed applicant for Acute QC Strut and Components?

The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Acute QC Strut and Components?

The FDA product code for Acute QC Strut and Components is OSN.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Smith & Nephew, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: OSN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.