K2M received FDA 510(k) clearance for additional implant sizes of its CASCADIA™ Lateral Interbody System.
CASCADIA, part of K2M’s minimally invasive spine portfolio, uses Lamellar 3D-printed Titanium Technology™ to create porous structures that support bony integration throughout the implant.
The CASCADIA family includes the CASCADIA TL, AN, AN Lordotic Oblique and Cervical Interbody systems.
Other device companies with lateral interbody offerings include Aurora Spine, ChoiseSpine, Life Spine, Medtronic, NuVasive, OsteoMed Spine, Tyber Medical, etc.
Sources: K2M, Inc.; FDA.gov; ORTHOWORLD Inc.
K2M received FDA 510(k) clearance for additional implant sizes of its CASCADIA™ Lateral Interbody System.
CASCADIA, part of K2M's minimally invasive spine portfolio, uses Lamellar 3D-printed Titanium Technology™ to create porous structures that support bony integration throughout the implant.
The CASCADIA family includes the...
K2M received FDA 510(k) clearance for additional implant sizes of its CASCADIA™ Lateral Interbody System.
CASCADIA, part of K2M’s minimally invasive spine portfolio, uses Lamellar 3D-printed Titanium Technology™ to create porous structures that support bony integration throughout the implant.
The CASCADIA family includes the CASCADIA TL, AN, AN Lordotic Oblique and Cervical Interbody systems.
Other device companies with lateral interbody offerings include Aurora Spine, ChoiseSpine, Life Spine, Medtronic, NuVasive, OsteoMed Spine, Tyber Medical, etc.
Sources: K2M, Inc.; FDA.gov; ORTHOWORLD Inc.
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JV
Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.




