The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Smith & Nephew, Inc Screw And Plate System Instrumentation.
Device ID | K123055 |
510k Number | K123055 |
Device Name: | SMITH & NEPHEW, INC SCREW AND PLATE SYSTEM INSTRUMENTATION |
Classification | Plate, Fixation, Bone |
Applicant | SMITH & NEPHEW, INC. 7135 Goodlett Farms Parkway Cordova, TN 38016 |
Contact | Bradley Heil |
Correspondent | Bradley Heil SMITH & NEPHEW, INC. 7135 Goodlett Farms Parkway Cordova, TN 38016 |
Product Code | HRS |
Subsequent Product Code | HTY |
Subsequent Product Code | HWC |
Subsequent Product Code | JDO |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-10-01 |
Decision Date | 2013-01-25 |
Summary: | summary |