The following data is part of a premarket notification filed by Ortho Development Corp. with the FDA for Ortho Development Balanced Knee System.
| Device ID | K994370 | 
| 510k Number | K994370 | 
| Device Name: | ORTHO DEVELOPMENT BALANCED KNEE SYSTEM | 
| Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer | 
| Applicant | ORTHO DEVELOPMENT CORP. 106 WEST 12200 SOUTH Draper, UT 84020 | 
| Contact | Carol Freasier | 
| Correspondent | Carol Freasier ORTHO DEVELOPMENT CORP. 106 WEST 12200 SOUTH 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 | 1999-12-27 | 
| Decision Date | 2000-03-24 | 
| Summary: | summary |