KINETIK GREAT TOE SYSTEM
K-Number: K924724 · 1994-01-05
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Device Summary
Frequently Asked Questions
What is the KINETIK GREAT TOE SYSTEM?
KINETIK GREAT TOE SYSTEM is a medical device that received FDA 510(k) clearance on 1994-01-05. The listed applicant is Kinetikos Medical, Inc.. The 510(k) number is K924724.
When did KINETIK GREAT TOE SYSTEM receive FDA 510(k) clearance?
KINETIK GREAT TOE SYSTEM received FDA 510(k) clearance on 1994-01-05, under 510(k) number K924724.
Who is the listed applicant for KINETIK GREAT TOE SYSTEM?
The FDA 510(k) record lists Kinetikos Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KINETIK GREAT TOE SYSTEM?
The FDA product code for KINETIK GREAT TOE 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 Kinetikos Medical, 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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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