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Food and Drug Administration / Food law / Neurosurgery / Medical device / Medical equipment / Spondylolisthesis / Federal Food /  Drug /  and Cosmetic Act / Premarket approval / Degenerative disc disease / Medicine / Health / Vertebral column


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Document Date: 2013-04-11 12:53:11


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City

Miami / /

Company

ulrich GmbH & Company KG / K123717 Trade / USA Inc. / /

Country

United States / /

Facility

New Hlampishire Avenue Document Control Center / /

/

IndustryTerm

announcements concerning your device / predicate devices / bone cement / manufacturing practice requirements / predicate systems / marketed predicate devices / manufacturing practice / cleared devices / fundamental scientific technology / /

MedicalCondition

osteopenia / spinal stenosis / degenerative disc disease / spinal tumor / degenerative scoliosis / kyphosis / spondylolisthesis / osteoporosis / spinal deformities / back pain / lordosis / /

MedicalTreatment

minimally invasive procedures / /

Organization

Center for Devices and Radiological Health / office of Compliance / office of Device Evaluation / office of Device Evaluation Center for Devices and Radiological Health Enclosure Indications for Use Statement / FDA / HUIIMAN SERVICES Public Health Service / New Hlampishire Avenue Document Control Center / Division of Postmarket You / Division of Orthopedic Devices / Division of Small Manufacturers / International and Consumer Assistance / DEPARTMENT OF HEALTH / Drug Administration / /

Person

Christy L.Foreman Christy Foreman / Hans Stover / Hans Stayer / /

/

Position

Director / /

ProgrammingLanguage

L / /

ProvinceOrState

Missouri / Maryland / /

Technology

radiation / fundamental scientific technology / /

URL

www.fda.gov/AboutFDA/CefltersOffices/CDRHI/CDR / /

SocialTag