Maxx Orthopedics, Inc.

Maxx Orthopedics, Inc. — FDA 510(k) Submissions

Maxx Orthopedics, Inc. has submitted 23 FDA 510(k) premarket notifications since 2009, of which 23 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer, Prosthesis, Knee, Patello/femorotibial, Semi-constrained, Uncemented, Porous, Coated, Polymer/metal/polymer, Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented, Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented, Hip, Semi-constrained, Cemented, Metal/ceramic/polymer + Additive, Porous Uncemented . Use the specialty filter in the sidebar to narrow results.