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 |