
SI-BONE, Inc.
Free shipping on orders over $99 · 30-day returns
iFuse TORQ® Implant System is an FDA 510(k)-cleared medical device (K231689) manufactured by SI-BONE, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 29, 2023. Regulation: 8.

Synthes (Usa)
SKU K100676
BackorderedMedline
SKU VM-1270020

Cardinal Health
SKU VM-1270026
BackorderedMoog
SKU VM-1270057