Knee+
K-Number: K233899 · 2024-03-08
ApplicantPixee Medical
Decision Date2024-03-08
Product CodeSBF
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Knee+ is a medical device manufactured by Pixee Medical. It received FDA 510(k) clearance on 2024-03-08 under approval number K233899. The device is classified under product code SBF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Knee+?
Knee+ is a medical device that received FDA 510(k) clearance on 2024-03-08. It is manufactured by Pixee Medical. The 510(k) number is K233899.
When was Knee+ approved by the FDA?
Knee+ received FDA 510(k) clearance on 2024-03-08, under approval number K233899.
What company makes Knee+?
Knee+ is manufactured by Pixee Medical.
What is the FDA product code for Knee+?
The FDA product code for Knee+ is SBF.
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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.