Knee+
K-Number: K230789 · 2023-04-21
Device Summary
Frequently Asked Questions
What is the Knee+?
Knee+ is a medical device that received FDA 510(k) clearance on 2023-04-21. The listed applicant is Pixee Medical. The 510(k) number is K230789.
When did Knee+ receive FDA 510(k) clearance?
Knee+ received FDA 510(k) clearance on 2023-04-21, under 510(k) number K230789.
Who is the listed applicant for Knee+?
The FDA 510(k) record lists Pixee Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Knee+?
The FDA product code for Knee+ is SBF.
Other records listing Pixee Medical as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: SBF)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.