The following data is part of a premarket notification filed by Hand Innovations, Inc. with the FDA for Distal Volar Radius Anatomical Plate System.
Device ID | K050932 |
510k Number | K050932 |
Device Name: | DISTAL VOLAR RADIUS ANATOMICAL PLATE SYSTEM |
Classification | Appliance, Fixation, Nail/blade/plate Combination, Multiple Component, Metal Composite |
Applicant | HAND INNOVATIONS, INC. 8905 SW 87TH AVENUE SUITE 220 Miami, FL 33176 |
Contact | Ernie Hernandez |
Correspondent | Ernie Hernandez HAND INNOVATIONS, INC. 8905 SW 87TH AVENUE SUITE 220 Miami, FL 33176 |
Product Code | LXT |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-04-14 |
Decision Date | 2005-04-26 |
Summary: | summary |