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U.S. Department of Health and Human Services

Product Classification

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Device filler, bone void, nonalterable compound for cranioplasty
Regulation Description Preformed nonalterable cranioplasty plate.
Definition A nonalterable cranial bone void filler is a device that is created from patient-specific computerized tomography (ct) imaging data and intended to fill bony voids, defects, and contour irregularities in non-load bearing regions of the cranial skeleton, and are not intrinsic to the stability of the bony structure.The materials used (e.G., metals, polyether ether ketone (peek), etc.) in the construction of the nonalterable cranial bone void fillers are not resorbable and cannot be altered or reshaped at the time of surgery or after implantation without changing the chemical behavior of the material.
Physical State Manufactured as Patient-Specific Preformed Implant
Technical Method The device is implanted in the bony void and may be secured using plates and screws to prevent the movement of the cranial bone void filler.
Target Area Cranium, Skull
Regulation Medical Specialty Neurology
Review Panel Neurology
Product CodePJN
Premarket Review Office of Device Evaluation (ODE)
Division of Neurological and Physical Medicine Devices (DNPMD)
Neurodiagnostic and Neurosurgical Devices Branch (NNDB)
Submission Type 510(k)
Regulation Number 882.5330
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Implanted Device? Yes
Life-Sustain/Support Device? No
Third Party Review Not Third Party Eligible