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 |