Smith&Nephew VISIONAIRE Patient Matched Cutting Blocks
K-Number: K200826 · 2020-04-24
ApplicantSmith & Nephew, Inc.
Decision Date2020-04-24
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Smith&Nephew VISIONAIRE Patient Matched Cutting Blocks is a medical device manufactured by Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2020-04-24 under approval number K200826. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by Smith & Nephew, Inc.. The 510(k) number is K200826.
When was Smith&Nephew VISIONAIRE Patient Matched Cutting Blocks approved by the FDA?
Smith&Nephew VISIONAIRE Patient Matched Cutting Blocks received FDA 510(k) clearance on 2020-04-24, under approval number K200826.
What company makes Smith&Nephew VISIONAIRE Patient Matched Cutting Blocks?
Smith&Nephew VISIONAIRE Patient Matched Cutting Blocks is manufactured by Smith & Nephew, Inc..
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.
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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.