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FDA 510(k)

MERETE TOEMOBILE ANATOMICAL GREAT TOE RESURFACING SYSTEM

K-Number: K072251 · 2008-05-08

Decision Date2008-05-08
Product CodeLZJ
DecisionSubstantially Equivalent

Device Summary

MERETE TOEMOBILE ANATOMICAL GREAT TOE RESURFACING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Merete Medical GmbH. It received FDA 510(k) clearance on 2008-05-08 under 510(k) number K072251. The device is classified under product code LZJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERETE TOEMOBILE ANATOMICAL GREAT TOE RESURFACING SYSTEM?

MERETE TOEMOBILE ANATOMICAL GREAT TOE RESURFACING SYSTEM is a medical device that received FDA 510(k) clearance on 2008-05-08. The listed applicant is Merete Medical GmbH. The 510(k) number is K072251.

When did MERETE TOEMOBILE ANATOMICAL GREAT TOE RESURFACING SYSTEM receive FDA 510(k) clearance?

MERETE TOEMOBILE ANATOMICAL GREAT TOE RESURFACING SYSTEM received FDA 510(k) clearance on 2008-05-08, under 510(k) number K072251.

Who is the listed applicant for MERETE TOEMOBILE ANATOMICAL GREAT TOE RESURFACING SYSTEM?

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

What is the FDA product code for MERETE TOEMOBILE ANATOMICAL GREAT TOE RESURFACING SYSTEM?

The FDA product code for MERETE TOEMOBILE ANATOMICAL GREAT TOE RESURFACING SYSTEM is LZJ.

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 Merete Medical GmbH 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: LZJ)

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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