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 |