Articulator Arthroscopic Bur
K-Number: K252666 · 2025-11-21
ApplicantJoint Preservation Innovations, LLC
Decision Date2025-11-21
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Articulator Arthroscopic Bur is a medical device manufactured by Joint Preservation Innovations, LLC. It received FDA 510(k) clearance on 2025-11-21 under approval number K252666. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Articulator Arthroscopic Bur?
Articulator Arthroscopic Bur is a medical device that received FDA 510(k) clearance on 2025-11-21. It is manufactured by Joint Preservation Innovations, LLC. The 510(k) number is K252666.
When was Articulator Arthroscopic Bur approved by the FDA?
Articulator Arthroscopic Bur received FDA 510(k) clearance on 2025-11-21, under approval number K252666.
What company makes Articulator Arthroscopic Bur?
Articulator Arthroscopic Bur is manufactured by Joint Preservation Innovations, LLC.
What is the FDA product code for Articulator Arthroscopic Bur?
The FDA product code for Articulator Arthroscopic Bur is HRX.
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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.