Mercury Medical Disposable Radiofrequency Cannula

FDA 510(k) K000073 · Mercury Medical

Substantially Equivalent

510(k) numberK000073

Submission

Device name
Mercury Medical Disposable Radiofrequency Cannula
Applicant
Mercury Medical
Middleton, MA, US
Received
January 10, 2000
Decision date
March 1, 2000
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GXI – Probe, Radiofrequency Lesion
Device class
Class II (moderate risk)
Regulation
21 CFR 882.4725
Specialty
Neurology

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K250213OptaBlate BVN Intraosseous Nerve Ablation System (10mm Probe Single Kit); OptaBlate BVN…GXI · Traditional Stryker Instruments05/15/2025SE
K241367RF CannulaGXI · Traditional Shanghai Samedical & Plastic Instruments Co., Ltd.01/23/2025SE
K222281Intracept Intraosseous Nerve Ablation SystemGXI · Traditional Relievant Medsystems, Inc.10/26/2022SE
K213836Intracept Intraosseous Nerve Ablation SystemGXI · Traditional Relievant Medsystems, Inc.03/11/2022SE
K203066COOLIEF Cooled Radiofrequency Kit AdvancedGXI · Traditional Avanos Medical, Inc.12/22/2020SE
K190259Vesta RF CannulaGXI · Special Biomerics02/07/2020SE

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Questions and answers

When was Mercury Medical Disposable Radiofrequency Cannula cleared by the FDA?

Mercury Medical Disposable Radiofrequency Cannula (K000073) received a 510(k) decision of Substantially Equivalent on March 1, 2000, 51 days after the submission was received.

What is the product code of K000073?

The FDA product code is GXI – Probe, Radiofrequency Lesion, a Class II (moderate risk) device regulated under 21 CFR 882.4725.