Neuropro Spinal Jaxx recalls

Neuropro Spinal Jaxx appears in 1 official U.S. recall notice indexed by RecallRadar, most recently on 2018-04-18.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• Spinal Jaxx Interbody Fusion Device, Model: 100001-511, Size: 9 H x 10 W x 25 L Product Usage: The Spinal Jaxx interbody fusion device is i…
  FDA Device · Class II · 2018-04-18 · Neuropro Spinal Jaxx