Pinnacle Spine Group, LLC
FDA 510(k) medical device clearances.
Top product codes for Pinnacle Spine Group, LLC
Recent clearances by Pinnacle Spine Group, LLC
- K172349 — InFill® Interbody Fusion Device
- K152259 — InFill Interbody Fusion Device
- K151184 — InFill Interbody Fusion Devices
- K150206 — InFill Interbody Fusion Devices
- K143488 — InFill Graft Delivery System
- K140066 — INFILL CERVICAL
- K133721 — INFILL 41-TLIF CONVEX OBLIQUE DEVICE, INFILL 43-TLIF CONTOUR OBLIQUE, INFILL 44-TLIF CONTOUR OBLIQUE AND THE INFILL 60
- K124012 — INFILL OBLIQUE TLIF DEVICE
- K121476 — INFILL GRAFT DELIVERY SYSTEM
- K121733 — INFILL INTERVERTEBRAL BODY FUSION DEVICE
- K111632 — INFILL GRAFT DELIVERY SYSTEM
- K103729 — INFILL INTERVERTEBRAL BODY FUSION DEVICE
Data sourced from openFDA. This site is unofficial and independent of the FDA.