Smith & Nephew VISIONAIRE Patient Matched Cutting Blocks
K-Number: K183010 · 2018-11-28
ApplicantSmith & Nephew, Inc.
Decision Date2018-11-28
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 2018-11-28 under approval number K183010. 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 2018-11-28. It is manufactured by Smith & Nephew, Inc.. The 510(k) number is K183010.
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 2018-11-28, under approval number K183010.
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.