The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Smith & Nephew Modular Hip.
Device ID | K042127 |
510k Number | K042127 |
Device Name: | SMITH & NEPHEW MODULAR HIP |
Classification | Prosthesis, Hip, Semi-constrained, Uncemented, Metal / Polymer, Non-porous, Calcium Phosphate |
Applicant | SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 |
Contact | Janet Johnson Akil |
Correspondent | Janet Johnson Akil SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 |
Product Code | MEH |
CFR Regulation Number | 888.3353 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-08-06 |
Decision Date | 2004-11-19 |
Summary: | summary |