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Knee+ — Pixee Medical (510(k) K230789)

Knee+ — Pixee Medical (510(k) K230789) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: Knee+; Applicant: Pixee Medical; Clearance track: 510(k).

Device nameKnee+
ApplicantPixee Medical
Clearance track510(k)
Submission numberK230789
DecisionSubstantially Equivalent
Decision date2023-04-21
Date received2023-03-22
Product codeSBF
Device class2
Medical specialtyNeurology
Applicant locationFR
SourceopenFDA device

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