CORIOGRAPH Knee Pre-Op Plan
K-Number: K240113 · 2024-03-18
ApplicantSmith & Nephew, Inc.
Decision Date2024-03-18
Product CodePBF
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
CORIOGRAPH Knee Pre-Op Plan is a medical device manufactured by Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2024-03-18 under approval number K240113. The device is classified under product code PBF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the CORIOGRAPH Knee Pre-Op Plan?
CORIOGRAPH Knee Pre-Op Plan is a medical device that received FDA 510(k) clearance on 2024-03-18. It is manufactured by Smith & Nephew, Inc.. The 510(k) number is K240113.
When was CORIOGRAPH Knee Pre-Op Plan approved by the FDA?
CORIOGRAPH Knee Pre-Op Plan received FDA 510(k) clearance on 2024-03-18, under approval number K240113.
What company makes CORIOGRAPH Knee Pre-Op Plan?
CORIOGRAPH Knee Pre-Op Plan is manufactured by Smith & Nephew, Inc..
What is the FDA product code for CORIOGRAPH Knee Pre-Op Plan?
The FDA product code for CORIOGRAPH Knee Pre-Op Plan is PBF.
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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.