Paragon T2 Wand with Integrated Cable
K-Number: K153675 · 2016-01-15
Device Summary
Frequently Asked Questions
What is the Paragon T2 Wand with Integrated Cable?
Paragon T2 Wand with Integrated Cable is a medical device that received FDA 510(k) clearance on 2016-01-15. The listed applicant is ArthroCare Corporation. The 510(k) number is K153675.
When did Paragon T2 Wand with Integrated Cable receive FDA 510(k) clearance?
Paragon T2 Wand with Integrated Cable received FDA 510(k) clearance on 2016-01-15, under 510(k) number K153675.
Who is the listed applicant for Paragon T2 Wand with Integrated Cable?
The FDA 510(k) record lists ArthroCare Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Paragon T2 Wand with Integrated Cable?
The FDA product code for Paragon T2 Wand with Integrated Cable is GEI.
Other records listing ArthroCare Corporation 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: GEI)
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.