KYPHON ANCHOR FACET SCREW SYSTEM— 510(k) K101765

Name: FDA 510(k) clearance K101765
Creator: U.S. Food and Drug Administration
Published: 2010-10-22

Substantially Equivalent

Medtronic Spine, LLC

FDA 510(k) clearance K101765 for KYPHON ANCHOR FACET SCREW SYSTEM, Substantially Equivalent on 2010-10-22. Applicant: Medtronic Spine, LLC. Device class: Unclassified.

Clearance details

Applicant: Medtronic Spine, LLC
Product code: Code MRW
Device class: Unclassified
Advisory panel: Unknown
Date received: 2010-06-23
Decision date: 2010-10-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sunnyvale, CA, US

Download summary PDF View on FDA.gov ↗

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