Adcura® Sagittae® Lateral Lumbar Interbody Fusion Devices
Adcura, Inc.
Adcura, Inc.
FDA Registration(s)#
| Registration | FEI | Name | Status | Initial importer | Expiration year | Address |
|---|---|---|---|---|---|---|
| 3013758617 | 3013758617 | Adcura, Inc. | 1 | N | 2026-01-01 | 18300 Minnetonka Blvd Ste 210 Wayzata MN US 55391 |
Registered Device Listings#
| Registration key | Listing key | Premarket submission | Device | Product code | Decision date |
|---|---|---|---|---|---|
| 226401 | 1721329197 | K223065 | Adcura® Sagittae® Lateral Lumbar Interbody Fusion Devices | MAX | 2022-10-26 |
| 226401 | 1047645936 | K200816 | SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices | MAX | 2020-04-30 |
| 226401 | 1266086789 | K190193 | SpineEX Sagittae® Lateral Lumbar Interbody Fusion Devices | MAX | 2019-03-04 |
| 226401 | 1281593856 | K181531 | SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices | MAX | 2018-10-05 |
Product Codes Associated With Registrations#
| Product code | Registration listing records | Latest decision |
|---|---|---|
| MAX | 4 | 2022-10-26 |