TOWNLEY FACET/PEDICULAR SCREW PLATING SYSTEM— 510(k) K953076

Name: FDA 510(k) clearance K953076
Creator: U.S. Food and Drug Administration
Published: 1997-02-28

Substantially Equivalent

Sofamor Danek USA,Inc.

FDA 510(k) clearance K953076 for TOWNLEY FACET/PEDICULAR SCREW PLATING SYSTEM, Substantially Equivalent on 1997-02-28. Applicant: Sofamor Danek USA,Inc.. Device class: Unclassified.

Clearance details

Applicant: Sofamor Danek USA,Inc.
Product code: Code MRW
Device class: Unclassified
Advisory panel: Unknown
Date received: 1995-06-30
Decision date: 1997-02-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Memphis, TN, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.