The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Smith & Nephew, Inc. Shoulder System Instruments.
| Device ID | K121714 | 
| 510k Number | K121714 | 
| Device Name: | SMITH & NEPHEW, INC. SHOULDER SYSTEM INSTRUMENTS | 
| Classification | Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented | 
| Applicant | SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 | 
| Contact | Bradley Heil | 
| Correspondent | Bradley Heil SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 | 
| Product Code | HSD | 
| CFR Regulation Number | 888.3690 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2012-06-11 | 
| Decision Date | 2012-09-07 | 
| Summary: | summary |