The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Echelon Porous Plus Ha Hip Stems.
Device ID | K023302 |
510k Number | K023302 |
Device Name: | ECHELON POROUS PLUS HA HIP STEMS |
Classification | Prosthesis, Hip, Semi-constrained, Uncemented, Metal / Polymer, Non-porous, Calcium Phosphate |
Applicant | SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 |
Contact | David Henley |
Correspondent | David Henley SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 |
Product Code | MEH |
CFR Regulation Number | 888.3353 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-10-03 |
Decision Date | 2002-10-25 |
Summary: | summary |