Cement, Bone, Vertebroplasty, Pre-formed, Modular

Device Code: 4654

Product Code(s): OBM

Definition: Reduction Of Vertebral Body Fractures In Conjunction With PMMA Bone Cement Cleared For Vertebroplasty And Restoration Of Vertebral Body Height.

Device Classification Information

Device Type ID4654
Device NameCement, Bone, Vertebroplasty, Pre-formed, Modular
Physical StateInterlocking Pre-formed PMMA Components Sized To The Desired Vertebral Body Dimensions
Technical MethodImplanted Modularly Within The Vertebral Body Until Desired Dimensions Are Achieved, Then Encapsulated In PMMA
Target AreaThoracic Or Lumbar Vertebral Bodies
Regulation DescriptionPolymethylmethacrylate (PMMA) Bone Cement.
Regulation Medical SpecialtyOrthopedic
Review PanelOrthopedic
Premarket Review Office Of Device Evaluation (ODE)
Division Of Orthopedic Devices (DOD)
Joint And Fixation Devices Branch One ¿ Knees/Shoulders/Elbows/Ankles/Toes (JFDB1)
Submission Type510(k)
CFR Regulation Number888.3027 [🔎]
FDA Device ClassificationClass 2 Medical Device
Product CodeOBM
GMP ExemptNo
Summary MREligible
Implanted DeviceYes
Life Support DeviceNo
Third Party Review Not Third Party Eligible

Recognized Standards

Total Product Life Cycle

Device Type ID4654
DeviceCement, Bone, Vertebroplasty, Pre-formed, Modular
Product CodeOBM
FDA Device ClassificationClass 2 Medical Device
Regulation DescriptionPolymethylmethacrylate (PMMA) Bone Cement.
CFR Regulation Number888.3027 [🔎]
TPLC Last Update: 2019-04-02 20:53:29

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.