The following data is part of a premarket notification filed by Ortho Development Corp. with the FDA for Ortho Development Balanced Knee Modular Tibial System.
Device ID | K031201 |
510k Number | K031201 |
Device Name: | ORTHO DEVELOPMENT BALANCED KNEE MODULAR TIBIAL SYSTEM |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | ORTHO DEVELOPMENT CORP. 12187 SOUTH BUSINESS PARK DR. Draper, UT 84020 |
Contact | Nadeem Ahmed |
Correspondent | Nadeem Ahmed ORTHO DEVELOPMENT CORP. 12187 SOUTH BUSINESS PARK DR. Draper, UT 84020 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-04-16 |
Decision Date | 2003-07-15 |
Summary: | summary |