The following data is part of a premarket notification filed by Zimmer, Inc. with the FDA for G7 Acetabular System Longevity Highly Crosslinked Polyethylene, G7 Acetabular System Vivacit-e Vitamin E Highly Crosslinked Polyethylene.
| Device ID | K190660 |
| 510k Number | K190660 |
| Device Name: | G7 Acetabular System Longevity Highly Crosslinked Polyethylene, G7 Acetabular System Vivacit-E Vitamin E Highly Crosslinked Polyethylene |
| Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
| Applicant | Zimmer, Inc. P.O. Box 708 Warsaw, IN 46581 -0708 |
| Contact | Mary Wentorf |
| Correspondent | Josh Davis Zimmer, Inc. P.O. Box 708 Warsaw, IN 46581 -0708 |
| Product Code | LPH |
| Subsequent Product Code | JDI |
| Subsequent Product Code | LZO |
| Subsequent Product Code | OQG |
| 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 | 2019-03-14 |
| Decision Date | 2019-12-05 |