The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Smith & Nephew, Inc. Intramedullary Nail System Instrumentation.
| Device ID | K122170 | 
| 510k Number | K122170 | 
| Device Name: | SMITH & NEPHEW, INC. INTRAMEDULLARY NAIL SYSTEM INSTRUMENTATION | 
| Classification | Rod, Fixation, Intramedullary And Accessories | 
| 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 | HSB | 
| Subsequent Product Code | HWC | 
| Subsequent Product Code | JDS | 
| Subsequent Product Code | KTT | 
| CFR Regulation Number | 888.3020 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2012-07-23 | 
| Decision Date | 2012-10-19 | 
| Summary: | summary |