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FDA 510(k)

GREAT TOE IMPLANT

K-Number: K920667 · 1992-06-19

ApplicantAcu Med, Inc.
Decision Date1992-06-19
Product CodeLZJ
DecisionSubstantially Equivalent

Device Summary

GREAT TOE IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Acu Med, Inc.. It received FDA 510(k) clearance on 1992-06-19 under 510(k) number K920667. The device is classified under product code LZJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GREAT TOE IMPLANT?

GREAT TOE IMPLANT is a medical device that received FDA 510(k) clearance on 1992-06-19. The listed applicant is Acu Med, Inc.. The 510(k) number is K920667.

When did GREAT TOE IMPLANT receive FDA 510(k) clearance?

GREAT TOE IMPLANT received FDA 510(k) clearance on 1992-06-19, under 510(k) number K920667.

Who is the listed applicant for GREAT TOE IMPLANT?

The FDA 510(k) record lists Acu Med, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GREAT TOE IMPLANT?

The FDA product code for GREAT TOE IMPLANT 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 Acu Med, Inc. 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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