The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Polarcup Dual Mobility System.
| Device ID | K110135 |
| 510k Number | K110135 |
| Device Name: | POLARCUP DUAL MOBILITY SYSTEM |
| Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
| Applicant | SMITH & NEPHEW, INC. 1450 EAST BROOKS RD. Memphis, TN 38116 |
| Contact | Theresa Leister |
| Correspondent | Theresa Leister SMITH & NEPHEW, INC. 1450 EAST BROOKS RD. Memphis, TN 38116 |
| Product Code | LPH |
| Subsequent Product Code | JDI |
| Subsequent Product Code | KWY |
| CFR Regulation Number | 888.3358 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-01-18 |
| Decision Date | 2011-10-14 |
| Summary: | summary |