The following data is part of a premarket notification filed by United Orthopedic Corp. with the FDA for Augment And Screw, Psa Type.
Device ID | K122183 |
510k Number | K122183 |
Device Name: | AUGMENT AND SCREW, PSA TYPE |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | UNITED ORTHOPEDIC CORP. 57 PARK AVE. 2, SCIENCE PARK Hsinchu, TW 300 |
Contact | Fang-yuan Ho |
Correspondent | Fang-yuan Ho UNITED ORTHOPEDIC CORP. 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 | 2012-07-23 |
Decision Date | 2013-02-05 |
Summary: | summary |