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 |