The following data is part of a premarket notification filed by United Orthopedic Corporation with the FDA for Ustar Ii System.
| Device ID | K190100 |
| 510k Number | K190100 |
| Device Name: | USTAR II System |
| Classification | Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/polymer |
| Applicant | United Orthopedic Corporation No 57, Park Ave 2, Science Park Hsinchu, TW 30075 |
| Contact | Lois Ho |
| Correspondent | Lois Ho United Orthopedic Corporation No 57, Park Ave 2, Science Park Hsinchu, TW 30075 |
| Product Code | KRO |
| Subsequent Product Code | KWL |
| Subsequent Product Code | LPH |
| Subsequent Product Code | LWJ |
| CFR Regulation Number | 888.3510 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-01-22 |
| Decision Date | 2019-09-23 |
| Summary: | summary |