ARTFX Lumbar PEEK Cages
K-Number: K240889 · 2024-10-02
ApplicantArtfx Medical
Decision Date2024-10-02
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
ARTFX Lumbar PEEK Cages is a medical device manufactured by Artfx Medical. It received FDA 510(k) clearance on 2024-10-02 under approval number K240889. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ARTFX Lumbar PEEK Cages?
ARTFX Lumbar PEEK Cages is a medical device that received FDA 510(k) clearance on 2024-10-02. It is manufactured by Artfx Medical. The 510(k) number is K240889.
When was ARTFX Lumbar PEEK Cages approved by the FDA?
ARTFX Lumbar PEEK Cages received FDA 510(k) clearance on 2024-10-02, under approval number K240889.
What company makes ARTFX Lumbar PEEK Cages?
ARTFX Lumbar PEEK Cages is manufactured by Artfx Medical.
What is the FDA product code for ARTFX Lumbar PEEK Cages?
The FDA product code for ARTFX Lumbar PEEK Cages is MAX.
Related Clinical Trials
Other Devices by Artfx Medical
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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.