Smith&Nephew VISIONAIRE Patient Matched Cutting Blocks
K-Number: K200826 · 2020-04-24
Device Summary
Frequently Asked Questions
What is the Smith&Nephew VISIONAIRE Patient Matched Cutting Blocks?
Smith&Nephew VISIONAIRE Patient Matched Cutting Blocks is a medical device that received FDA 510(k) clearance on 2020-04-24. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K200826.
When did Smith&Nephew VISIONAIRE Patient Matched Cutting Blocks receive FDA 510(k) clearance?
Smith&Nephew VISIONAIRE Patient Matched Cutting Blocks received FDA 510(k) clearance on 2020-04-24, under 510(k) number K200826.
Who is the listed applicant for Smith&Nephew VISIONAIRE Patient Matched Cutting Blocks?
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 Smith&Nephew VISIONAIRE Patient Matched Cutting Blocks?
The FDA product code for Smith&Nephew VISIONAIRE Patient Matched Cutting Blocks is JWH.
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: JWH)
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.