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# K2M Gains Clearance for Expandable Interbody System
- URL: https://www.fdaweb.com/k2m-gains-clearance-for-expandable-interbody-system/
- Published: 2017-06-22T12:00:00.000Z
- Updated: 2026-09-14T22:30:54.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5139007

FDA has cleared a K2M Group Holdings 510(k) for its Mojave PL 3D Expandable Interbody System, a 3D-printed expandable posterior-lumbar interbody system that features the company’s [Lamellar 3D Titanium Technology](https://www.globenewswire.com/Tracker?data=xf1ydVo8D-XPrQ6rXqSf6Mey4exXbeyLPaahO8BfNOZh-IFHSSHxEO6I5rV00s8xHODSifhZWXpEKh0sx1H1DRxlGyMV0A%5F0E1dHX4hPhyWtPFY5gniINTZSMLDbtGe0aL4EzNOBt3-SLtLA7sCXhMZ-D2kCafYe%5Fdu%5F8cP3HMF1mr4OktFaOVGcipGzlcwo&ref=fdaweb.com). The fusion device is designed to allow for independent control of the anterior and posterior height in the lumbar spine, the company says. a “Featuring infinite adjustment within the expansion range, the implant may be locked at any desired height and lordosis to aid in the restoration of sagittal balance,” it adds.