Anterior Cervical Plate

CastleLoc-P

The CastleLoc-P Anterior Cervical Plate System offers surgeons simplicity, efficiency and versatility. CastleLoc-P Anterior Cervical Plate System is a low profile system that offers surgeons the option of a constrained or semi-constrained construct. CastleLoc-P is composed of Titanium Alloy (Ti-6Al- 4V-ELI), and it features a simple locking mechanism and large visualization windows for great intra-operative and post-operative view of the graft site.

Features:

The CastleLoc-P Anterior Cervical Plate System is an anterior cervical spinal fixation device made from titanium alloy (Ti-6Al-4V). Plates are available in one through four level configurations. The system also includes variable bone screws available in several diameters and lengths.

Locking Mechanism

The thread conical screw head locks to the plate, eliminating the need for an additional locking or blocking mechanism.

It prevents screw pull-out from plate up to 126N.

Plates

  • Slim and Low-Profile (17 mm x 1.7 mm)
  • 1-4 Level Fusion

Bone Screws

  • Screw Lengths from 12 mm to 20 mm, in 1 mm increment
  • 3.5 mm/ 4.0 mm diameters
  • Self-Tapping/ Self-Drilling/ Fixed/ Variable

Indication

CastleLoc-P Anterior Cervical Plate System is intended for anterior screw fixation to the cervical spine (C2-C7). CastleLoc-P Anterior Cervical Plate System is indicated for use in the immobilization and stabilization of the spine as an adjunct to fusions in patients with:

  • Degenerative Disc Disease (as defined by neck pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies)
  • Spondylolisthesis
  • Trauma (i.e. fractures or dislocations)
  • Tumors
  • Deformity (defined as kyphosis, lordosis, or scoliosis)
  • Pseuodarthrosis
  • Failed previous fusion
  • Spinal Stenosis

Contraindications

  • Active systemic infection or an infection localized to the site of the proposed implantation
  • Severe osteoporosis may prevent adequate fixation of screws and thus preclude the use of this or any other spinal instrumentation system
  • Patients who have been shown to be safely and predictably treated without internal fixation
  • Open wounds

CAUTION: THIS PRODUCT IS CLASSIFIED AS A MEDICAL DEVICE. IT IS RECOMMENDED TO READ THE INSTRUCTIONS CAREFULLY BEFORE USE.