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FDA 510(k)

MultiFIX S Ultra Knotless Fixation System

K-Number: K153669 · 2016-01-19

ApplicantArthocare Corporation
Decision Date2016-01-19
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MultiFIX S Ultra Knotless Fixation System is a medical device manufactured by Arthocare Corporation. It received FDA 510(k) clearance on 2016-01-19 under approval number K153669. 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 MultiFIX S Ultra Knotless Fixation System?

MultiFIX S Ultra Knotless Fixation System is a medical device that received FDA 510(k) clearance on 2016-01-19. It is manufactured by Arthocare Corporation. The 510(k) number is K153669.

When was MultiFIX S Ultra Knotless Fixation System approved by the FDA?

MultiFIX S Ultra Knotless Fixation System received FDA 510(k) clearance on 2016-01-19, under approval number K153669.

What company makes MultiFIX S Ultra Knotless Fixation System?

MultiFIX S Ultra Knotless Fixation System is manufactured by Arthocare Corporation.

What is the FDA product code for MultiFIX S Ultra Knotless Fixation System?

The FDA product code for MultiFIX S Ultra Knotless Fixation System is MBI.

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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.

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