3 FDA updates for spine, orthopedic technologies in 3 days

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Here are three spine and orthopedic tools and implants that have earned FDA clearances and updates in the past three days, as reported by Becker’s

  1. Medtech company Propiro earned FDA clearance for its Picasso feature within its Paradigm platform.
  2. Orthopedic implant company Miach Orthopaedics received 510(k) clearance from the FDA to update labeling of its BEAR knee implant. 
  3. VySpine’s VyBrate VBR system earned the FDA’s 510(k) clearance.

At the Becker’s 32nd Annual Meeting: The Business and Operations of ASCs, taking place October 29-31 in Chicago, ASC leaders, surgeons and healthcare executives will explore strategies to drive growth, enhance operational performance, navigate reimbursement challenges and prepare for the future of ambulatory surgery. Apply for complimentary registration now.

Register to Attend Webinar

Is ambulatory care healthcare’s big margin engine? 4 leaders weigh in

Wednesday, July 29
1:00 PM - 2:00 PM CDT

Presenters: Joe Ganley, athenahealthJeffrey Flynn, CASC, Gramercy Surgery CenterBryan Tsao, Access Center, Loma Linda University HealthJason Zepeda, Northridge Hospital Medical Center, CommonSpirit HealthGreg DeConciliis, PA-C, CASC, Boston Out­Patient Surgical Suites

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