Woven Orthopedics receives FDA 510(k) clearance of implant enhancement system

Fact checked byGina Brockenbrough, MA

Key takeaways:

FDA 510(k) clearance of the Ogmend implant enhancement system clears the system for use during orthopedic spine surgery.
The Ogmend system aids in screw fixation to allow for proper bone healing.

Woven Orthopedic Technologies has announced FDA 510(k) clearance of the Ogmend implant enhancement system to help surgeons achieve strong screw fixation during spine surgery, according to a press release.

The Ogmend system facilitates bone healing by securing screws into bone, according to the release.

FDA HQ in Washington — Woven Orthopedic Technologies received FDA 510(k) clearance of the Ogmend implant enhancement system. *Image: Adobe Stock*

“We are thrilled to deliver surgeons a simple, reliable solution to help overcome one of the most prevalent yet least discussed challenges in orthopedic and spine surgery: the ability to more confidently use surgical screws when operating in compromised fixation scenarios,” Brandon Bendes, co-founder and president of Woven Orthopedics, said in the release.

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Woven Orthopedics receives FDA 510(k) clearance of implant enhancement system

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