The following data is part of a premarket notification filed by Hand Innovations, Inc. with the FDA for Distal Radius Fracture Repair System.
| Device ID | K032705 |
| 510k Number | K032705 |
| Device Name: | DISTAL RADIUS FRACTURE REPAIR 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 | Al Weisenborn |
| Correspondent | Al Weisenborn 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 | 2003-09-02 |
| Decision Date | 2003-10-01 |
| Summary: | summary |