ACUMED ANATOMIC RADIAL HEAD SYSTEM
K-Number: K041858 · 2004-10-05
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Device Summary
Frequently Asked Questions
What is the ACUMED ANATOMIC RADIAL HEAD SYSTEM?
ACUMED ANATOMIC RADIAL HEAD SYSTEM is a medical device that received FDA 510(k) clearance on 2004-10-05. The listed applicant is Acumed, LLC. The 510(k) number is K041858.
When did ACUMED ANATOMIC RADIAL HEAD SYSTEM receive FDA 510(k) clearance?
ACUMED ANATOMIC RADIAL HEAD SYSTEM received FDA 510(k) clearance on 2004-10-05, under 510(k) number K041858.
Who is the listed applicant for ACUMED ANATOMIC RADIAL HEAD 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 ANATOMIC RADIAL HEAD SYSTEM?
The FDA product code for ACUMED ANATOMIC RADIAL HEAD SYSTEM is KWI.
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: KWI)
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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