The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Reflection Cross-linked Uhmwpe Acetabular Components.
Device ID | K002747 |
510k Number | K002747 |
Device Name: | REFLECTION CROSS-LINKED UHMWPE ACETABULAR COMPONENTS |
Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
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 | LPH |
CFR Regulation Number | 888.3358 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-09-05 |
Decision Date | 2000-12-15 |