OSMA Events

WHEN: Wednesday, January 26 & Thursday, January 27, 2022 WHERE: Zoom – links will be distributed before the meeting REGISTRATION: https://www.eventbrite.com/e/o… SPEAKER QUESTIONS: Submit to mpc@osma.net no later than December 23, 2021.

WHERE: Webex OSMA Member Registration: https://www.eventbrite.com/e/o… Speaker questions can be submitted to mpc@osma.net with FALL QUESTIONS in the subject line. Please send your questions in no later than Friday, October 22nd.

Registration is now open for the OSMA Summer Meeting https://osmasummer21.eventbrit… agenda agenda

Register Now: https://osmasp2021.eventbrite….

Register now: https://www.eventbrite.com/e/o…  

FDA has announced the first of a series of workshops focused on improving public understanding of infections related to orthopaedic devices, including mitigation measures and the promotion of public health in this clinical area. This workshop will explore new and ongoing research, discuss potential strategies to address associated challenges, develop innovative solutions and foster collaboration […]

Virtual Meeting Thursday, October 29 9:00 a.m. – 4:00 p.m. EDT OSMA Business Meeting MDSAP Experience Discussion ASME V&V40 Highlights from the FDA Spinal Devices Premarket Review Workshop Friday, October 30 8:00 a.m. – 5:00 p.m. EDT FDA Presentations: OHT6 Update Bone Void Fillers Safety and Performance Based Guidance Biocompatibility and Sterility NESTcc Use Cases […]

FDA has published dates for the next meeting of the Orthopaedic and Rehabilitation Devices Panel. The Panel will convene via an online platform on Tuesday, September 8th and Wednesday, September 9th. Per the announcement, “during session 1, the committee will discuss and make recommendations regarding the classification of facet screws systems which are currently unclassified […]

The Food and Drug Administration (FDA) is announcing a public workshop entitled “Spinal Device Premarket Review.” The workshop is intended to enhance public understanding of FDA’s review of data and information submitted to support premarket authorization for spinal devices falling under 21 CFR 888.3070 and 21 CFR 888.3080 by highlighting key sections of a 510(k) […]