LIGAMAX 5
K-Number: K110699 · 2011-03-25
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Device Summary
Frequently Asked Questions
What is the LIGAMAX 5?
LIGAMAX 5 is a medical device that received FDA 510(k) clearance on 2011-03-25. The listed applicant is Ethicon Endo-Sugery, LLC. The 510(k) number is K110699.
When did LIGAMAX 5 receive FDA 510(k) clearance?
LIGAMAX 5 received FDA 510(k) clearance on 2011-03-25, under 510(k) number K110699.
Who is the listed applicant for LIGAMAX 5?
The FDA 510(k) record lists Ethicon Endo-Sugery, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIGAMAX 5?
The FDA product code for LIGAMAX 5 is FZP.
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 Ethicon Endo-Sugery, 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: FZP)
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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