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 |