The following data is part of a premarket notification filed by United Orthopedic Corporation with the FDA for U2 Femoral Head.
Device ID | K162957 |
510k Number | K162957 |
Device Name: | U2 Femoral Head |
Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
Applicant | UNITED ORTHOPEDIC CORPORATION NO 57, PARK AVE 2, SCIENCE PARK Hsinchu, TW 300 |
Contact | Gimpel Chien |
Correspondent | Gimpel Chien UNITED ORTHOPEDIC CORPORATION NO 57, PARK AVE 2, SCIENCE PARK Hsinchu, TW 300 |
Product Code | LPH |
CFR Regulation Number | 888.3358 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-10-24 |
Decision Date | 2017-07-17 |
Summary: | summary |