The following data is part of a premarket notification filed by Biomet Manufacturing Corp. with the FDA for Taperloc Complete Size 4mm And Xr 123.
Device ID | K120030 |
510k Number | K120030 |
Device Name: | TAPERLOC COMPLETE SIZE 4MM AND XR 123 |
Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
Applicant | BIOMET MANUFACTURING CORP. 56 EAST BELL DRIVE P.O. BOX 587 Warsaw, IN 46581 -0587 |
Contact | Becky Earl |
Correspondent | Becky Earl BIOMET MANUFACTURING CORP. 56 EAST BELL DRIVE P.O. BOX 587 Warsaw, IN 46581 -0587 |
Product Code | LPH |
Subsequent Product Code | JDI |
Subsequent Product Code | KWL |
Subsequent Product Code | KWY |
Subsequent Product Code | KWZ |
Subsequent Product Code | LZO |
Subsequent Product Code | MEH |
Subsequent Product Code | OQG |
CFR Regulation Number | 888.3358 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-01-04 |
Decision Date | 2012-08-17 |
Summary: | summary |