The following data is part of a premarket notification filed by Wright Medical Technology, Inc. with the FDA for Darco Small Screw.
Device ID | K082320 |
510k Number | K082320 |
Device Name: | DARCO SMALL SCREW |
Classification | Screw, Fixation, Bone |
Applicant | WRIGHT MEDICAL TECHNOLOGY, INC. 5677 AIRLINE RD. Arlington, TN 38002 |
Contact | Sarah Holtgrewe |
Correspondent | Sarah Holtgrewe 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 | 2008-08-13 |
Decision Date | 2008-11-05 |
Summary: | summary |