MultiFIX S Ultra Knotless Fixation System
K-Number: K153669 · 2016-01-19
Device Summary
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. The listed applicant is Arthocare Corporation. The 510(k) number is K153669.
When did MultiFIX S Ultra Knotless Fixation System receive FDA 510(k) clearance?
MultiFIX S Ultra Knotless Fixation System received FDA 510(k) clearance on 2016-01-19, under 510(k) number K153669.
Who is the listed applicant for MultiFIX S Ultra Knotless Fixation System?
The FDA 510(k) record lists Arthocare Corporation as the applicant. This does not by itself establish the device manufacturer.
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.
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.
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.