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FDA 510(k)

MITEK MINI QUICKANCHOR PLUS

K-Number: K992487 · 1999-09-21

Decision Date1999-09-21
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MITEK MINI QUICKANCHOR PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Mitek Products. It received FDA 510(k) clearance on 1999-09-21 under 510(k) number K992487. 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 MITEK MINI QUICKANCHOR PLUS?

MITEK MINI QUICKANCHOR PLUS is a medical device that received FDA 510(k) clearance on 1999-09-21. The listed applicant is Mitek Products. The 510(k) number is K992487.

When did MITEK MINI QUICKANCHOR PLUS receive FDA 510(k) clearance?

MITEK MINI QUICKANCHOR PLUS received FDA 510(k) clearance on 1999-09-21, under 510(k) number K992487.

Who is the listed applicant for MITEK MINI QUICKANCHOR PLUS?

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

What is the FDA product code for MITEK MINI QUICKANCHOR PLUS?

The FDA product code for MITEK MINI QUICKANCHOR PLUS is HWC. This falls under the Cardiovascular category.

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 Mitek Products 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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Related Devices (Code: HWC)

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

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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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