The following data is part of a premarket notification filed by Wright Medical Technology, Inc. with the FDA for Distal Radius Fracture Fixation Plate System.
| Device ID | K943853 |
| 510k Number | K943853 |
| Device Name: | DISTAL RADIUS FRACTURE FIXATION PLATE SYSTEM |
| Classification | Plate, Fixation, Bone |
| Applicant | WRIGHT MEDICAL TECHNOLOGY, INC. 5677 AIRLINE RD. Arlington, TN 38002 |
| Contact | Dan Regan |
| Correspondent | Dan Regan WRIGHT MEDICAL TECHNOLOGY, INC. 5677 AIRLINE RD. Arlington, TN 38002 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-08-08 |
| Decision Date | 1995-01-20 |