ACUMED CONGRUENT BONE PLATE SYSTEM
K-Number: K063460 · 2006-12-07
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Device Summary
Frequently Asked Questions
What is the ACUMED CONGRUENT BONE PLATE SYSTEM?
ACUMED CONGRUENT BONE PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2006-12-07. The listed applicant is Acumed, LLC. The 510(k) number is K063460.
When did ACUMED CONGRUENT BONE PLATE SYSTEM receive FDA 510(k) clearance?
ACUMED CONGRUENT BONE PLATE SYSTEM received FDA 510(k) clearance on 2006-12-07, under 510(k) number K063460.
Who is the listed applicant for ACUMED CONGRUENT BONE PLATE SYSTEM?
The FDA 510(k) record lists Acumed, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACUMED CONGRUENT BONE PLATE SYSTEM?
The FDA product code for ACUMED CONGRUENT BONE PLATE 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 Acumed, LLC 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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