This page includes the latest FDA filings for Akros Medical. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3013401747 |
| FEI Number | 3013401747 |
| Name | AKROS MEDICAL |
| Owner & Operator | Akros Medical |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 3503 Pleasant Green Rd Durham, NC 27705 US |
| Establishment Type | Complaint File Establishment per 21 CFR 820.198 |
Device Company | Device | Date |
|---|---|---|
Akros Medical | Akros Scruture Anchor LisFranc Repair Kit | 2020-04-06 |
AKROS MEDICAL | FibuLink | 2020-03-24 |
AKROS MEDICAL | FibuLink | 2020-03-24 |
Akros Medical | Akros FibuLink™ Syndesmosis Repair Kit | 2017-12-14 |
AKROS MEDICAL | FibuLink | 2017-01-23 |
Akros Medical | Akros Fibulink Syndesmosis Repair Kit | 2017-01-10 |