ARTHREX INTERFERENCE SCREW
K-Number: K062466 · 2006-11-29
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Device Summary
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.
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
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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