The following data is part of a premarket notification filed by United Orthopedic Corporation with the FDA for U2 Bipolar Implant And 22mm Femoral Head.
Device ID | K152439 |
510k Number | K152439 |
Device Name: | U2 Bipolar Implant And 22mm Femoral Head |
Classification | Prosthesis, Hip, Hemi-, Femoral, Metal/polymer, Cemented Or Uncemented |
Applicant | UNITED ORTHOPEDIC CORPORATION NO 57, PARK AVE 2, SCIENCE PARK Hsinchu, TW 300 |
Contact | Karen Ho |
Correspondent | Karen Ho UNITED ORTHOPEDIC CORPORATION NO 57, PARK AVE 2, SCIENCE PARK Hsinchu, TW 300 |
Product Code | KWY |
CFR Regulation Number | 888.3390 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-08-27 |
Decision Date | 2016-04-07 |
Summary: | summary |