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- 12:00 p.m. Preliminary study results indicate that X-BOLT Orthopaedics' X-BOLT device for hip fracture repair demonstrated a cut-out rate of 0.8% in a population of 476 patients, and performed as well as a hip sliding screw in measures such as quality of life, mortality, revision, etc.
- 11:45 a.m. Camber Spine launched the SPIRA-O® Open Matrix OLIF device in the U.S.
- Wright Medical completed enrollment of 500 patients in its U.K.-based postmarket INFINITY™ Total Ankle follow-up study.
Articles of Interest All Articles
FDA 510(k) Recap: Spinal Devices and Technologies from 1H19
In considering that the NASS 2019 Annual Meeting is weeks away, we thought it an ideal time to revisit spine products that have gained FDA 510(k) clearance in the first half of the year. This round-up shares another entrant into the SI joint arena, a first clearance for an enabling technology for a company that already has implants on the market and additional details about some lesser-known companies to watch.
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