The following data is part of a premarket notification filed by Darco International, Inc. with the FDA for Darco Locking Bone Plate System.
Device ID | K061808 |
510k Number | K061808 |
Device Name: | DARCO LOCKING BONE PLATE SYSTEM |
Classification | Plate, Fixation, Bone |
Applicant | DARCO INTERNATIONAL, INC. 810 MEMORIAL BLVD. Huntington, WV 25701 |
Contact | Mark S Cooper |
Correspondent | Mark S Cooper DARCO INTERNATIONAL, INC. 810 MEMORIAL BLVD. Huntington, WV 25701 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-06-27 |
Decision Date | 2006-08-17 |
Summary: | summary |