KIRSCHNER SUPER-FIXATION SYSTEM— 510(k) K881896

Name: FDA 510(k) clearance K881896
Creator: U.S. Food and Drug Administration
Published: 1988-07-28

Substantially Equivalent

Kirschner Medical Corp.

FDA 510(k) clearance K881896 for KIRSCHNER SUPER-FIXATION SYSTEM, Substantially Equivalent on 1988-07-28. Applicant: Kirschner Medical Corp.. Device class: 2.

Clearance details

Applicant: Kirschner Medical Corp.
Product code: Code JEC
Device class: Class 2
Regulation: 21 CFR 888.3040
Advisory panel: Orthopedic
Date received: 1988-05-05
Decision date: 1988-07-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Timonium, MD, US

Download summary PDF View on FDA.gov ↗

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