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FDA 510(k)

TRIDENT ANCHOR

K-Number: K060914 · 2006-06-09

ApplicantJohnson & Johnson Company
Decision Date2006-06-09
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TRIDENT ANCHOR is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Company. It received FDA 510(k) clearance on 2006-06-09 under 510(k) number K060914. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIDENT ANCHOR?

TRIDENT ANCHOR is a medical device that received FDA 510(k) clearance on 2006-06-09. The listed applicant is Johnson & Johnson Company. The 510(k) number is K060914.

When did TRIDENT ANCHOR receive FDA 510(k) clearance?

TRIDENT ANCHOR received FDA 510(k) clearance on 2006-06-09, under 510(k) number K060914.

Who is the listed applicant for TRIDENT ANCHOR?

The FDA 510(k) record lists Johnson & Johnson Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRIDENT ANCHOR?

The FDA product code for TRIDENT ANCHOR is HWC. This falls under the Cardiovascular category.

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Other records listing Johnson & Johnson Company 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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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