Life Spine announced that its FS3 Posterior MIS Screw System received 510(k) clearance from US FDA.
The FS3 MIS Spinal System offers cannulated wire guided Minimally Invasive Surgery implants and instrumentation for accommodating a range of patient pathologies either in open surgery or percutaneous. Its intuitive design allows for fast, reliable, and reproducible access and implantation with minimal exposure and tissue dissection.
Michael S. Butler, Life Spine’s President and CEO stated, This is the first of many new minimally invasive innovations that Life Spine is bringing to market over the next six months. In addition to our already diverse product offering, the FS3 posterior MIS screw system marks our fourteenth product to market and further strengthens our position as an engineering centric operation focused on bringing surgeon concepts to life.