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 |