The following data is part of a premarket notification filed by United Orthopedic Corporation with the FDA for U2 Tibial Baseplate- Cma Type, Tibial Insert And Augment.
Device ID | K131864 |
510k Number | K131864 |
Device Name: | U2 TIBIAL BASEPLATE- CMA TYPE, TIBIAL INSERT AND AUGMENT |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | UNITED ORTHOPEDIC CORPORATION NO 57, PARK AVE 2, SCIENCE PARK Hsinchu, TW 300 |
Contact | Fang-yuan Ho |
Correspondent | Fang-yuan Ho UNITED ORTHOPEDIC CORPORATION NO 57, PARK AVE 2, SCIENCE PARK Hsinchu, TW 300 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-06-24 |
Decision Date | 2014-01-15 |
Summary: | summary |