The following data is part of a premarket notification filed by Biomet Manufacturing Corp. with the FDA for Biomet Femoral Locking Nail System.
Device ID | K072161 |
510k Number | K072161 |
Device Name: | BIOMET FEMORAL LOCKING NAIL SYSTEM |
Classification | Rod, Fixation, Intramedullary And Accessories |
Applicant | BIOMET MANUFACTURING CORP. PO BOX 587 Warsaw, IN 46581 -0587 |
Contact | Becky Earl |
Correspondent | Becky Earl BIOMET MANUFACTURING CORP. PO BOX 587 Warsaw, IN 46581 -0587 |
Product Code | HSB |
CFR Regulation Number | 888.3020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-08-06 |
Decision Date | 2007-09-20 |
Summary: | summary |