FDA clears Stryker's Lite lumbar plating system

Stryker has the FDA's 510(k) clearance for a new spinal repair device, the Lite plate system for lumbar fusion procedures.

Stryker (NYSE:SYK) added another product to its spine division, following a new 510(k) clearance from the FDA.

American Academy of Orthopedic Surgeons (AAOS), Food & Drug Administration (FDA), Stryker

News Well, 510(k), Orthopedics, Regulatory/Compliance, Spinal

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