The following data is part of a premarket notification filed by Wright Medical Technology, Inc. with the FDA for Advance Less Conforming Tibial Component.
Device ID | K030193 |
510k Number | K030193 |
Device Name: | ADVANCE LESS CONFORMING TIBIAL COMPONENT |
Classification | Prosthesis, Knee, Femorotibial, Semi-constrained, Cemented, Metal/polymer |
Applicant | WRIGHT MEDICAL TECHNOLOGY, INC. 5677 AIRLINE RD. Arlington, TN 38002 |
Contact | Tim Crabtree |
Correspondent | Tim Crabtree WRIGHT MEDICAL TECHNOLOGY, INC. 5677 AIRLINE RD. Arlington, TN 38002 |
Product Code | HRY |
CFR Regulation Number | 888.3530 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-01-21 |
Decision Date | 2003-02-20 |
Summary: | summary |