FDA 510(k)

Smith & Nephew ACCORD Cable System

K-Number: K223762 · 2023-05-30

Decision Date2023-05-30

Product CodeHRS

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Smith & Nephew ACCORD Cable System is a medical device manufactured by Smith & Nephew. It received FDA 510(k) clearance on 2023-05-30 under approval number K223762. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Smith & Nephew ACCORD Cable System?

Smith & Nephew ACCORD Cable System is a medical device that received FDA 510(k) clearance on 2023-05-30. It is manufactured by Smith & Nephew. The 510(k) number is K223762.

When was Smith & Nephew ACCORD Cable System approved by the FDA?

Smith & Nephew ACCORD Cable System received FDA 510(k) clearance on 2023-05-30, under approval number K223762.

What company makes Smith & Nephew ACCORD Cable System?

Smith & Nephew ACCORD Cable System is manufactured by Smith & Nephew.

What is the FDA product code for Smith & Nephew ACCORD Cable System?

The FDA product code for Smith & Nephew ACCORD Cable System is HRS.

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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.