The following data is part of a premarket notification filed by Wright Medical Technology, Inc. with the FDA for Darco Headed Cannulated Screw.
| Device ID | K100359 |
| 510k Number | K100359 |
| Device Name: | DARCO HEADED CANNULATED SCREW |
| Classification | Screw, Fixation, Bone |
| Applicant | WRIGHT MEDICAL TECHNOLOGY, INC. 5677 AIRLINE RD. Arlington, TN 38002 |
| Contact | Kelsey Lee |
| Correspondent | Kelsey Lee WRIGHT MEDICAL TECHNOLOGY, INC. 5677 AIRLINE RD. Arlington, TN 38002 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-02-12 |
| Decision Date | 2010-06-24 |
| Summary: | summary |