Knee Arthroplasty Implantation System

What Is This Device?

Intended to be used to assist in the implantation of a specific knee arthroplasty device or a set of specific knee arthroplasty devices. Indicated to include guiding alignment, making or establishing cuts, selecting, sizing, attaching, positioning or orienting implant components.

What Is FDA Product Code OOG?

Knee Arthroplasty Implantation System is FDA product code OOG, Class 2, 21 CFR 888.3560.

How Does It Reach the US Market?

A 510(k) premarket notification is required before it is sold in the United States: the applicant shows the device is substantially equivalent to one already on the market. No clearance under this code names a Chinese applicant. A registration is not a clearance: the plants above are set up to make it, and the 510(k) it is sold under is held by whoever files it, often the brand.

What Do the Recalls Say?

The FDA has recorded 3 recalls under this product code since 2015. None was by a company in China. The root cause the FDA records most often is Process design (3).

A recall is a fact about one product and its maker, not a grade for every manufacturer of the type.