Pinnacle Spine Group, LLC
Pinnacle Spine Group, LLC holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2017.
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.