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 |