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510(k) Data Aggregation

K Number

Device Name

KYPHON ANCHOR FACET SCREW SYSTEM

Manufacturer

MEDTRONIC SPINE LLC.

Date Cleared

2010-10-22

(121 days)

Product Code

Regulation Number

N/A

Why did this record match?

Applicant Name (Manufacturer) :

MEDTRONIC SPINE LLC.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

Device Description

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