Key Highlights
- Vy Spine receives FDA clearance for LumiVy OsteoVy PEKK Lumbar IBF.
- Device designed for lumbar intervertebral body fusion for levels L2 to S1.
- 3D printed OXPEKK technology supports osseointegration and bony integration.
- Available in a range of sizes, lordosis options, and self-drilling screws.
- Ideal for patients with metal hypersensitivity due to bacterostatic properties.
Source: Business Wire
Notable Quotes
- “The LumiVy OsteoVy PEKK Lumbar IBF clearance is another product in a long line of Vy Spine implants which will utilize the unique qualities of our proprietary OsteoVy PEKK designs.” — Bret Berry, President of Product Development at Vy Spine
- “We are confident that the combination of OPM’s novel 3D printed PEKK technology and Vy Spine’s unique designs & experience within the spine marketplace will drive substantial adoption of this best-in-class solution.” — Scott DeFelice, CEO at Oxford Performance Materials
SoHC's Take
The FDA clearance of Vy Spine’s LumiVy OsteoVy PEKK Lumbar IBF represents a significant advancement in spinal care, utilizing cutting-edge 3D printed technology for enhanced patient outcomes. The use of OXPEKK, known for its superior osseointegration and compatibility with metal-sensitive patients, positions this device as a leader in the lumbar interbody fusion market. The variety of implant options and design flexibility further supports its adoption across diverse clinical needs, emphasizing Vy Spine’s commitment to innovation and patient-centered care.
