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 |