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# OrthoGrid Systems PhantomMSK Trauma Cleared
- URL: https://www.fdaweb.com/orthogrid-systems-phantommsk-trauma-cleared/
- Published: 2019-12-10T12:00:00.000Z
- Updated: 2026-09-14T15:56:00.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5145691

FDA has cleared an OrthoGrid Systems 510(k) for its application PhantomMSK Trauma for use in orthopedic surgery. The universal software platform is intended to work with all manufacturer devices across multiple procedures using fluoroscopic imaging to assist with implant, instrument and anatomic alignment, the company says. It has software features and proprietary algorithms to correct fluoroscopic image distortion. “To operate PhantomMSK Trauma, a fluoroscopic image is acquired from a C-arm displayed outside the sterile field, where the image analysis tools can be used at the surgeon’s discretion,” OrthoGrid says.