Acute QC Strut and Components
K-Number: K221792 · 2022-08-25
ApplicantSmith & Nephew, Inc.
Decision Date2022-08-25
Product CodeOSN
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Acute QC Strut and Components is a medical device manufactured by Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2022-08-25 under approval 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. It is manufactured by Smith & Nephew, Inc.. The 510(k) number is K221792.
When was Acute QC Strut and Components approved by the FDA?
Acute QC Strut and Components received FDA 510(k) clearance on 2022-08-25, under approval number K221792.
What company makes Acute QC Strut and Components?
Acute QC Strut and Components is manufactured by Smith & Nephew, Inc..
What is the FDA product code for Acute QC Strut and Components?
The FDA product code for Acute QC Strut and Components is OSN.
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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.