The following data is part of a premarket notification filed by Stelkast Company with the FDA for Proven Knee System.
| Device ID | K000113 |
| 510k Number | K000113 |
| Device Name: | PROVEN KNEE SYSTEM |
| Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
| Applicant | STELKAST COMPANY 800 VINIAL STREET, SUITE B-210 Pittsburgh, PA 15212 |
| Contact | Donald A Stevens |
| Correspondent | Donald A Stevens STELKAST COMPANY 800 VINIAL STREET, SUITE B-210 Pittsburgh, PA 15212 |
| Product Code | JWH |
| CFR Regulation Number | 888.3560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-01-14 |
| Decision Date | 2000-04-04 |