TAPERLOC COMPLETE MICROPLASTY STEM
K-Number: K110400 · 2011-09-30
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Device Summary
Frequently Asked Questions
What is the TAPERLOC COMPLETE MICROPLASTY STEM?
TAPERLOC COMPLETE MICROPLASTY STEM is a medical device that received FDA 510(k) clearance on 2011-09-30. The listed applicant is Biomet Manufacturing Corp. The 510(k) number is K110400.
When did TAPERLOC COMPLETE MICROPLASTY STEM receive FDA 510(k) clearance?
TAPERLOC COMPLETE MICROPLASTY STEM received FDA 510(k) clearance on 2011-09-30, under 510(k) number K110400.
Who is the listed applicant for TAPERLOC COMPLETE MICROPLASTY STEM?
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 TAPERLOC COMPLETE MICROPLASTY STEM?
The FDA product code for TAPERLOC COMPLETE MICROPLASTY STEM 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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