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 |