Dakota LP System
FDA 510(k) K250769 · Precision Spine, Inc.
510(k) numberK250769
Submission
- Device name
- Dakota LP System
- Applicant
- Precision Spine, Inc.
Pear, MS, US - Received
- March 13, 2025
- Decision date
- November 24, 2025
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- ODP – Intervertebral Fusion Device With Bone Graft, Cervical
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3080
- Specialty
- Orthopedic
- Implant
- Yes
Intended to stabilize cervical spinal segment to promote fusion in order to restrict motion and decrease pain using bone graft.
Other 510(k)s with product code ODP
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K262595 | VariLift-C Cervical Interbody Fusion SystemODP · Special | Wenzel Spine, Inc. | 08/26/2026SE |
| K262489 | BluEX Cervical Expandable Cage SystemODP · Special | L&K BIOMED Co., Ltd. | 08/18/2026SE |
| K253041 | 3d Cage CervicalODP · Traditional | Fims Co., Ltd. | 07/23/2026SE |
| K262061 | Tritanium® C Anterior Cervical Cage; Tritanium® PL Cage; Tritanium® TL Curved Posterior…ODP · Special | Stryker Spine | 07/17/2026SE |
| K254130 | C.A. Medical Interbody Fusion SystemODP · Special | C.A. Medical, LLC | 07/08/2026SE |
| K260840 | BluEX Cervical Expandable Cage SystemODP · Traditional | L&K BIOMED Co., Ltd. | 05/16/2026SE |
| K260850 | Osteomni Spinal Cages SystemODP · Traditional | Osteomni, Inc. | 05/12/2026SE |
| K260549 | ZSFab Cervical Interbody System and ZSFab Lumbar Interbody SystemODP · Special | Zsfab, Inc. | 04/24/2026SE |
| K253260 | ORIO-3D Cage SystemODP · Traditional | SpineCraft | 04/16/2026SE |
| K260340 | HC Biologics Osteopoint PEEK Cages, HC Biologics Osteopoint Cervical PEEK Cages, HC…ODP · Traditional | HC Biologics, LLC | 04/13/2026SE |
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| K213118 | Dakota ALIF SystemOVD · Traditional | 04/01/2022SE |
| K220324 | AccuFit Lateral 2-Hole PlateKWQ · Traditional | 03/16/2022SE |
| K212075 | ShurFit Lumbar Interbody SystemMAX · Traditional | 12/08/2021SE |
| K212937 | Dakota ALIF Plate SystemKWQ · Traditional | 11/04/2021SE |
| K203129 | NexGen Standalone Anterior Cervical Discectomy and Fusion (ACDF) SystemOVE · Traditional | 01/12/2021SE |
| K200303 | Reform Pedicle Screw SystemNKB · Traditional | 05/19/2020SE |
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Questions and answers
When was Dakota LP System cleared by the FDA?
Dakota LP System (K250769) received a 510(k) decision of Substantially Equivalent on November 24, 2025, 256 days after the submission was received.
What is the product code of K250769?
The FDA product code is ODP – Intervertebral Fusion Device With Bone Graft, Cervical, a Class II (moderate risk) device regulated under 21 CFR 888.3080.