KINETIK GREAT TOE SYSTEM— 510(k) K924724

Name: FDA 510(k) clearance K924724
Creator: U.S. Food and Drug Administration
Published: 1994-01-05

Substantially Equivalent

Kinetikos Medical, Inc.

FDA 510(k) clearance K924724 for KINETIK GREAT TOE SYSTEM, Substantially Equivalent on 1994-01-05. Applicant: Kinetikos Medical, Inc.. Device class: Unclassified.

Clearance details

Applicant: Kinetikos Medical, Inc.
Product code: Code LZJ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1992-09-21
Decision date: 1994-01-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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