Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LIGAMAX 5

K-Number: K110699 · 2011-03-25

Decision Date2011-03-25
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIGAMAX 5 is the device name listed in this FDA 510(k) record. The listed applicant is Ethicon Endo-Sugery, LLC. It received FDA 510(k) clearance on 2011-03-25 under 510(k) number K110699. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

↑