ACUMED WRIST ARTHRODESIS PLATE SYSTEM
K-Number: K100123 · 2010-10-06
Advertisement
Device Summary
Frequently Asked Questions
What is the ACUMED WRIST ARTHRODESIS PLATE SYSTEM?
ACUMED WRIST ARTHRODESIS PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2010-10-06. The listed applicant is Acumed, LLC. The 510(k) number is K100123.
When did ACUMED WRIST ARTHRODESIS PLATE SYSTEM receive FDA 510(k) clearance?
ACUMED WRIST ARTHRODESIS PLATE SYSTEM received FDA 510(k) clearance on 2010-10-06, under 510(k) number K100123.
Who is the listed applicant for ACUMED WRIST ARTHRODESIS 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 WRIST ARTHRODESIS PLATE SYSTEM?
The FDA product code for ACUMED WRIST ARTHRODESIS 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.
Advertisement