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 |