The following data is part of a premarket notification filed by Zimmer, Inc. with the FDA for Epoch Hip Prosthesis, Model 4075 Series.
| Device ID | K014070 |
| 510k Number | K014070 |
| Device Name: | EPOCH HIP PROSTHESIS, MODEL 4075 SERIES |
| Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
| Applicant | ZIMMER, INC. P.O. BOX 708 Warsaw, IN 46581 -0708 |
| Contact | Karen Cain |
| Correspondent | Karen Cain ZIMMER, INC. P.O. BOX 708 Warsaw, IN 46581 -0708 |
| Product Code | LPH |
| CFR Regulation Number | 888.3358 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-12-10 |
| Decision Date | 2002-07-30 |
| Summary: | summary |