FDA 510(k)

ARTHROCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM (MODEL 970)

K-Number: K961747 · 1996-07-15

Decision Date1996-07-15

Product CodeHRX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

ARTHROCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM (MODEL 970) is the device name listed in this FDA 510(k) record. The listed applicant is Arthrocare Corp.. It received FDA 510(k) clearance on 1996-07-15 under 510(k) number K961747. 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 ARTHROCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM (MODEL 970)?

ARTHROCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM (MODEL 970) is a medical device that received FDA 510(k) clearance on 1996-07-15. The listed applicant is Arthrocare Corp.. The 510(k) number is K961747.

When did ARTHROCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM (MODEL 970) receive FDA 510(k) clearance?

ARTHROCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM (MODEL 970) received FDA 510(k) clearance on 1996-07-15, under 510(k) number K961747.

Who is the listed applicant for ARTHROCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM (MODEL 970)?

The FDA 510(k) record lists Arthrocare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTHROCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM (MODEL 970)?

The FDA product code for ARTHROCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM (MODEL 970) is HRX.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.