The following data is part of a premarket notification filed by Maxx Orthopedics, Inc. with the FDA for Freedom Pck Components.
| Device ID | K131481 |
| 510k Number | K131481 |
| Device Name: | FREEDOM PCK COMPONENTS |
| Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
| Applicant | MAXX ORTHOPEDICS, INC. 531 PLYMOUTH RD., SUITE 526 Plymouth Meeting, PA 19462 |
| Contact | Nach Dave |
| Correspondent | Nach Dave MAXX ORTHOPEDICS, INC. 531 PLYMOUTH RD., SUITE 526 Plymouth Meeting, PA 19462 |
| Product Code | JWH |
| CFR Regulation Number | 888.3560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-05-22 |
| Decision Date | 2014-02-21 |
| Summary: | summary |