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FDA 510(k)

ARTHREX INTERFERENCE SCREW

K-Number: K062466 · 2006-11-29

ApplicantArthrex, Inc.
Decision Date2006-11-29
Product CodeMAI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHREX INTERFERENCE SCREW is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 2006-11-29 under 510(k) number K062466. The device is classified under product code MAI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHREX INTERFERENCE SCREW?

ARTHREX INTERFERENCE SCREW is a medical device that received FDA 510(k) clearance on 2006-11-29. The listed applicant is Arthrex, Inc.. The 510(k) number is K062466.

When did ARTHREX INTERFERENCE SCREW receive FDA 510(k) clearance?

ARTHREX INTERFERENCE SCREW received FDA 510(k) clearance on 2006-11-29, under 510(k) number K062466.

Who is the listed applicant for ARTHREX INTERFERENCE SCREW?

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

What is the FDA product code for ARTHREX INTERFERENCE SCREW?

The FDA product code for ARTHREX INTERFERENCE SCREW is MAI.

Related Clinical Trials

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.

Other records listing Arthrex, Inc. 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.

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Related Devices (Code: MAI)

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

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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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