Understanding Testing Requirements for Additive Orthopedic Devices

About Webinar

Introducing additive manufacturing technology into your existing, new or custom product lines creates additional challenges when bringing your product to market. Understanding how the technology impacts your R&D testing and validation is critical to a successful product launch. As a worldwide leader in both materials and product level testing, join Element to review testing best practices for additive implants, updates on standards, and additional requirements to consider when evaluating your additively manufactured products.

About speaker/s

Maciej Jakucki, Medical Device Manager, Element Materials Technology

Mr. Jakucki has performed and managed a wide variety of medical testing projects and programs to meet FDA and CE requirements, with a decade of experience working in the medical device and pharmaceutical industries. He is an active ASTM member and routinely contributes to driving the industry forward. He has performed submission testing both domestically and internationally for hundreds of active products across the spine, joint arthroplasty, maxillofacial and trauma industries.

No matter your station in the orthopedic commercialization chain — engineer, executive, buyer, surgeon, investor, inventor, manufacturer — OMTEC is your resource.