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FDA 510(k)

MAGNUM M FIXATION DEVICE

K-Number: K090380 · 2009-03-13

ApplicantArthrocare Corp.
Decision Date2009-03-13
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MAGNUM M FIXATION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Arthrocare Corp.. It received FDA 510(k) clearance on 2009-03-13 under 510(k) number K090380. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGNUM M FIXATION DEVICE?

MAGNUM M FIXATION DEVICE is a medical device that received FDA 510(k) clearance on 2009-03-13. The listed applicant is Arthrocare Corp.. The 510(k) number is K090380.

When did MAGNUM M FIXATION DEVICE receive FDA 510(k) clearance?

MAGNUM M FIXATION DEVICE received FDA 510(k) clearance on 2009-03-13, under 510(k) number K090380.

Who is the listed applicant for MAGNUM M FIXATION DEVICE?

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 MAGNUM M FIXATION DEVICE?

The FDA product code for MAGNUM M FIXATION DEVICE is MBI.

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Other records listing Arthrocare Corp. as applicant

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Related Devices (Code: MBI)

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.

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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.

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