Acute QC Strut and Components
K-Number: K221792 · 2022-08-25
Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.