Reform Ti Modular

Device typeSpinal fixation implant/sterilization container set: A collection of non-sterile, implantable components of an internal spinal fixation assembly (e.g., plates, rods, screws, connectors, and/or hooks) packaged within a reusable sterilization container (i.e., all under the same product code) to be sterilized prior to implantation. The set provides the surgeon with a selection of implants (e.g., different sizes) during surgery, whereby unused implants may be resterilised for subsequent implantation in another patient. Instruments intended to facilitate implantation may be packaged with the set. This is a reusable device which includes single-use implants.

FDA categoryBone Cement, Posterior Screw Augmentation, Material, External Aesthetic Restoration, No Adhesive

Device ID00840019971386

Catalog number39-SF-9560

AvailabilityPrescription

Single useYes

MRI safetyLabeling does not contain MRI Safety Information