The following data is part of a premarket notification filed by Dow Corning Wright with the FDA for Kim Modular Femoral Hip Prosthesis.
| Device ID | K895399 |
| 510k Number | K895399 |
| Device Name: | KIM MODULAR FEMORAL HIP PROSTHESIS |
| Classification | Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented |
| Applicant | DOW CORNING WRIGHT P.O. BOX 100 Arlington, TN 38002 |
| Contact | Bailey Lipscomb |
| Correspondent | Bailey Lipscomb DOW CORNING WRIGHT P.O. BOX 100 Arlington, TN 38002 |
| Product Code | LZO |
| CFR Regulation Number | 888.3353 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-09-07 |
| Decision Date | 1989-12-14 |