The following data is part of a premarket notification filed by Zimmer, Inc. with the FDA for Trilogy Acetabular System.
Device ID | K934765 |
510k Number | K934765 |
Device Name: | TRILOGY ACETABULAR SYSTEM |
Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
Applicant | ZIMMER, INC. P.O. BOX 708 Warsaw, IN 46581 -0708 |
Contact | Angie Ide |
Correspondent | Angie Ide 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 | 1993-10-05 |
Decision Date | 1994-04-29 |