ARCOS INTERLOCKING DISTAL STEMS
K-Number: K100469 · 2010-12-07
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Device Summary
Frequently Asked Questions
What is the ARCOS INTERLOCKING DISTAL STEMS?
ARCOS INTERLOCKING DISTAL STEMS is a medical device that received FDA 510(k) clearance on 2010-12-07. The listed applicant is Biomet Manufacturing Corp. The 510(k) number is K100469.
When did ARCOS INTERLOCKING DISTAL STEMS receive FDA 510(k) clearance?
ARCOS INTERLOCKING DISTAL STEMS received FDA 510(k) clearance on 2010-12-07, under 510(k) number K100469.
Who is the listed applicant for ARCOS INTERLOCKING DISTAL STEMS?
The FDA 510(k) record lists Biomet Manufacturing Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARCOS INTERLOCKING DISTAL STEMS?
The FDA product code for ARCOS INTERLOCKING DISTAL STEMS is KWA.
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 Biomet Manufacturing Corp 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: KWA)
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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