Smith & Nephew ACCORD™ Cable System
K-Number: K223762 · 2023-05-30
Device Summary
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. The listed applicant is Smith & Nephew. The 510(k) number is K223762.
When did Smith & Nephew ACCORD™ Cable System receive FDA 510(k) clearance?
Smith & Nephew ACCORD™ Cable System received FDA 510(k) clearance on 2023-05-30, under 510(k) number K223762.
Who is the listed applicant for Smith & Nephew ACCORD™ Cable System?
The FDA 510(k) record lists Smith & Nephew as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Smith & Nephew ACCORD™ Cable System?
The FDA product code for Smith & Nephew ACCORD™ Cable System is HRS.
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 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: HRS)
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.