Implantology Corp.

Implantology Corp. — FDA 510(k) Submissions

Implantology Corp. has submitted 9 FDA 510(k) premarket notifications since 1993, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prosthesis, Hip, Femoral Component, Cemented, Metal, Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer, Prosthesis, Hip, Semi-constrained (metal Cemented Acetabular Component), Prosthesis, Hip, Semi-constrained, Uncemented, Metal / Polymer, Non-porous, Calcium Phosphate, Prosthesis, Hip, Hemi-, Femoral, Metal Ball . Use the specialty filter in the sidebar to narrow results.