The following data is part of a premarket notification filed by Biomet, Inc. with the FDA for G7 Osseoti Acetublar Shells.
Device ID | K140669 |
510k Number | K140669 |
Device Name: | G7 OSSEOTI ACETUBLAR SHELLS |
Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
Applicant | BIOMET, INC. 56 EAST BELL DR. BOX 587 Warsaw, IN 46581 -0587 |
Contact | Becky Earl |
Correspondent | Becky Earl BIOMET, INC. 56 EAST BELL DR. BOX 587 Warsaw, IN 46581 -0587 |
Product Code | LPH |
Subsequent Product Code | JDI |
Subsequent Product Code | KWZ |
Subsequent Product Code | LZO |
Subsequent Product Code | OQG |
Subsequent Product Code | OQH |
Subsequent Product Code | OQI |
Subsequent Product Code | PBI |
CFR Regulation Number | 888.3358 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-03-18 |
Decision Date | 2014-12-11 |
Summary: | summary |