COMPREHENSIVEPROXIMAL HUMERAL PLATING SYSTEM
K-Number: K110320 · 2011-07-21
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Device Summary
Frequently Asked Questions
What is the COMPREHENSIVEPROXIMAL HUMERAL PLATING SYSTEM?
COMPREHENSIVEPROXIMAL HUMERAL PLATING SYSTEM is a medical device that received FDA 510(k) clearance on 2011-07-21. The listed applicant is Biomet Manufacturing Corp. The 510(k) number is K110320.
When did COMPREHENSIVEPROXIMAL HUMERAL PLATING SYSTEM receive FDA 510(k) clearance?
COMPREHENSIVEPROXIMAL HUMERAL PLATING SYSTEM received FDA 510(k) clearance on 2011-07-21, under 510(k) number K110320.
Who is the listed applicant for COMPREHENSIVEPROXIMAL HUMERAL PLATING SYSTEM?
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 COMPREHENSIVEPROXIMAL HUMERAL PLATING SYSTEM?
The FDA product code for COMPREHENSIVEPROXIMAL HUMERAL PLATING SYSTEM is HRS.
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: HRS)
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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