Spinal Elements, Inc - TiBond - Class 2 Recall

Ti-Bond Marketing Literature/Labeling, Catalog No. LT10000, MP-14000 This device is intended to be used with autogenous bone graft. Patients must have undergone a regimen of at least six (6) months non-operative treatment prior to being treated with this device.
Source: Medical Device Recalls - Category: Medical Equipment Source Type: alerts