QVI

Screw Sleeve Bone Fixation Device, Spine

Product code
QVI
Device name
Screw Sleeve Bone Fixation Device, Spine
Device class
Class 2
21 CFR
21 CFR 888.3043
Medical specialty
Orthopedic
Marketing pathway
510(K)
Flag
Implant
510(k) clearances (last 3 years)
2

FDA classification definition

A spinal screw sleeve bone fixation device is intended to be implanted in conjunction with a non-resorbable, metallic bone screw where the screw has lost purchase due to loosening, backout, or breakage. The device fits between the screw threads and surrounding bone, and provides increased surface area to create an interference fit to restore stability of the implant construct.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

510(k) clearances, last 3 years (1)

Last three years. Most recent: 2023-10-26.

NumberDecision dateApplicantDevice nameSummary
K2332232023-10-26Woven Orthopedic TechnologiesOGmend® Implant Enhancement SystemFDA
Official FDA classification page: QVI
Classification and pathway per current FDA publications. Data from openFDA (CC0).