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# FDA Clears Lantheus Bone Scan Index
- URL: https://www.fdaweb.com/fda-clears-lantheus-bone-scan-index/
- Published: 2020-11-13T12:00:00.000Z
- Updated: 2026-09-14T16:36:22.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5148084

FDA has granted 510(k) clearance for the use of Lantheus’ artificial intelligence-enabled automated bone scan index product on the GE Healthcare Xelerix platform. The company [describes](https://www.marketwatch.com/press-release/lantheus-holdings-announces-fda-clearance-for-ai-enabled-automated-bone-scan-index-absi-in-prostate-cancer-on-ge-healthcares-xeleris-platform-2020-11-13?tesla=y&ref=fdaweb.com) it as a vendor-neutral standalone software as a medical device that calculates the automated bone scan index in Technetium-99m bone scintigraphy. The product was cleared by FDA in 2019.