The following data is part of a premarket notification filed by Zimmer, Inc. with the FDA for Vivacit-e Vitamin E Highly Crosslinked Polyethylene Liners.
| Device ID | K120370 |
| 510k Number | K120370 |
| Device Name: | VIVACIT-E VITAMIN E HIGHLY CROSSLINKED POLYETHYLENE LINERS |
| Classification | Hip Prosthesis, Semi-constrained, Cemented, Metal/polymer, + Additive, Porous, Uncemented |
| Applicant | ZIMMER, INC. 1800 WEST CENTER STREET Warsaw, IN 46580 |
| Contact | Rebecca Brook |
| Correspondent | Rebecca Brook ZIMMER, INC. 1800 WEST CENTER STREET Warsaw, IN 46580 |
| Product Code | OQG |
| Subsequent Product Code | JDI |
| Subsequent Product Code | LPH |
| Subsequent Product Code | LZO |
| Subsequent Product Code | OQH |
| Subsequent Product Code | OQI |
| CFR Regulation Number | 888.3358 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-02-06 |
| Decision Date | 2012-06-04 |
| Summary: | summary |