The following data is part of a premarket notification filed by Biomet Microfixation with the FDA for Biomet Microfixation Neuro Plating System.
Device ID | K121624 |
510k Number | K121624 |
Device Name: | BIOMET MICROFIXATION NEURO PLATING SYSTEM |
Classification | Plate, Cranioplasty, Preformed, Alterable |
Applicant | BIOMET MICROFIXATION 1520 TRADEPORT DR. Jacksonville, FL 32218 |
Contact | Sheryl Malmberg |
Correspondent | Sheryl Malmberg BIOMET MICROFIXATION 1520 TRADEPORT DR. Jacksonville, FL 32218 |
Product Code | GWO |
Subsequent Product Code | GXR |
Subsequent Product Code | HBW |
CFR Regulation Number | 882.5320 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-06-01 |
Decision Date | 2012-10-12 |
Summary: | summary |