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www.fdanews.com/articles/190638-fda-clears-implanets-screw-securing-device-for-vertebral-fusion

FDA Clears Implanet’s Screw Securing Device for Vertebral Fusion 

March 20, 2019

The FDA granted Implanet 510(k) clearance for another product in the company’s Jazz product range, the Jazz Cap system, a device used for securing screws in poor-quality bone.

The product consists of a set of single-use sterile implants that support the treatment of degenerative conditions in patients.

The implants are composed of a band, a screw, and the company’s patented locking mechanism.

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