FDA 510(k) Applications Submitted by Eric Linder
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K210402 |
02/10/2021 |
Curiteva Sacroiliac Joint Fusion System |
Curiteva, Inc. |
| K250845 |
03/20/2025 |
Curiteva Porous PEEK Standalone ALIF System |
Curiteva, Inc. |
| K231232 |
04/28/2023 |
Curiteva Laminoplasty System |
Curiteva, Inc. |
| K181261 |
05/11/2018 |
Curiteva Cervical Interbody Fusion System |
Curiteva, LLC |
| K181549 |
06/12/2018 |
Curiteva Midline Anterior Cervical Plate System (or Curiteva Anterior Cervical Plate System) |
Curiteva, LLC |
| K181562 |
06/14/2018 |
Curiteva Anterior Cervical Plate System |
Curiteva, LLC |
| K181589 |
06/18/2018 |
Curiteva Lumbar Interbody Fusion System |
Curiteva, LLC |
| K191810 |
07/05/2019 |
Curiteva Pedicle Screw System |
Curiteva, Inc. |
| K213030 |
09/21/2021 |
Curiteva Porous PEEK Cervical Interbody Fusion System |
Curiteva, Inc. |
| K233360 |
09/29/2023 |
Curiteva Thoracolumbar Plate System |
Curiteva, Inc. |
| K243137 |
09/30/2024 |
Curiteva Porous PEEK Laminoplasty System |
Curiteva, Inc. |
| K223200 |
10/13/2022 |
Curiteva Navigation System |
Curiteva, Inc. |
| K233744 |
11/22/2023 |
Curiteva Porous PEEK Lumbar Interbody Fusion System |
Curiteva, Inc. |
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