UNIVERSAL EXTERNAL FIXATION ASSEMBLY— 510(k) K790262

Name: FDA 510(k) clearance K790262
Creator: U.S. Food and Drug Administration
Published: 1979-02-13

Substantially Equivalent

Zimmer, Inc.

FDA 510(k) clearance K790262 for UNIVERSAL EXTERNAL FIXATION ASSEMBLY, Substantially Equivalent on 1979-02-13. Applicant: Zimmer, Inc.. Device class: 2.

Clearance details

Applicant: Zimmer, Inc.
Product code: Code JEC
Device class: Class 2
Regulation: 21 CFR 888.3040
Advisory panel: Orthopedic
Date received: 1979-02-06
Decision date: 1979-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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