ACUMED WRIST SPANNING PLATE
K-Number: K131764 · 2013-09-05
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Device Summary
Frequently Asked Questions
What is the ACUMED WRIST SPANNING PLATE?
ACUMED WRIST SPANNING PLATE is a medical device that received FDA 510(k) clearance on 2013-09-05. The listed applicant is Acumed, LLC. The 510(k) number is K131764.
When did ACUMED WRIST SPANNING PLATE receive FDA 510(k) clearance?
ACUMED WRIST SPANNING PLATE received FDA 510(k) clearance on 2013-09-05, under 510(k) number K131764.
Who is the listed applicant for ACUMED WRIST SPANNING PLATE?
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 SPANNING PLATE?
The FDA product code for ACUMED WRIST SPANNING PLATE 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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