MODIFICATION TO: SATELLITE SPINAL SYSTEM— 510(k) K060415

Name: FDA 510(k) clearance K060415
Creator: U.S. Food and Drug Administration
Published: 2007-01-05

Unknown

Medtronic Sofamor Danek

FDA 510(k) clearance K060415 for MODIFICATION TO: SATELLITE SPINAL SYSTEM, Unknown on 2007-01-05. Applicant: Medtronic Sofamor Danek. Device class: 3.

Clearance details

Applicant: Medtronic Sofamor Danek
Product code: Code NVR
Device class: Class 3
Advisory panel: Unknown
Date received: 2006-02-17
Decision date: 2007-01-05
Decision: Unknown
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.