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Food and Drug Administration / Orthopedic surgery / Spinal fusion / Degenerative disc disease / Medical device / Spondylolisthesis / Federal Food / Drug / and Cosmetic Act / Center for Devices and Radiological Health / Back pain / Medicine / Vertebral column / Neurosurgery


Document Date: 2014-08-08 12:37:10

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City

Mequon / /

Company

Titan Spine LLC / Nuvasive / Service cFodand lDng Administration Titan Spine LLC / /

Country

United States / /

Event

FDA Phase / /

/

IndustryTerm

subject device / announcements concerning your device / predicate devices / body fusion device / Internet address http /

MedicalCondition

IBD / Degenerative Disc Disease / discogenic back pain / I spondylolisthesis / /

MedicalTreatment

spinal surgery / /

Organization

Orthopedic Devices Office / Division of Postmarket Surveillance / Division of Industry and Consumer Education / Center for Devices and Radiological Health / Food and Drug Administration office of Chief Information officer Paperwork Reduction Act / office of Surveillance / FDA / Department of Health and Human Services / Sfor Mark N. Melkerson Director Division / Device Evaluation Center for Devices and Radiological Health Enclosure / /

Person

Ronald P.Jean -Sfor / Jane Rodd / Christine Scifert / Christine Scifert Memphis / Mark N. Melkerson / /

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Product

Federal Food / to / Endloskeleton® TO / Endloskeleton / /

ProvinceOrState

Tennessee / Wisconsin / /

Technology

radiation / /

URL

www.fda.azov/Medica / http /

SocialTag