BOCA RATON, Fla.--(BUSINESS WIRE)--SurGenTec, a privately held medical device company focusing on spine and orthopedic technologies, proudly announces FDA clearance for TiLink-P, a first-of-its-kind, ...

BURLINGAME, Calif., Jan. 25, 2024 /PRNewswire/ --.CoherentMI published a report, titled, Global Sacroiliac Joint Fusion Market was valued at US$ 625.3 Million in the year 2023 and is anticipated to ...

Current evidence on the safety and efficacy of minimally invasive sacroiliac (SI) joint fusion surgery for chronic SI pain is adequate to support the use of this procedure provided that standard ...

1. Tenon Medical earned FDA 510(k) clearance to use its Catamaran sacroiliac joint system for augmenting thoracolumbar fusion. The indication was first used in June by Andrew Trontis, MD. 2. A new ...

Sacroiliac joint fusion has historically been an overlooked opportunity for ASCs. That’s where SI-BONE’s iFuse Implant System® comes into play. Designed to permanently stabilize the sacroiliac (SI) ...

DEL MAR, Calif.--(BUSINESS WIRE)--SAIL Fusion, a medical device company focused on advancing the surgical treatment of sacroiliac joint dysfunction through solutions built upon AO principles, today ...

AUSTIN, Texas, Feb. 6, 2026 /PRNewswire/ -- Genesys Spine today announced the results of a prospective multicenter clinical study evaluating the safety and effectiveness of the SIros ® Lateral ...

Humana is one of the 5 largest commercial payors in the U.S. and joins 36 other commercial health plans that offer coverage for the triangular iFuse Implant System only SANTA CLARA, Calif., Dec. 16, ...

New positive coverage policy is specific for FDA cleared implants placed across the SI joint and intended to promote bone fusion SANTA CLARA, Calif., Dec. 13, 2019 (GLOBE NEWSWIRE) -- SI-BONE, Inc., ...

This section describes safety outcomes from the published literature that the committee considered as part of the evidence about this procedure. For more detailed information on the evidence, see the ...