Align Cervical Interbody Fusion System
FDA 510(k) K230639 · Acuity Surgical Devices, LLC
510(k) numberK230639
Submission
- Device name
- Align Cervical Interbody Fusion System
- Applicant
- Acuity Surgical Devices, LLC
Irving, TX, US - Received
- March 8, 2023
- Decision date
- December 1, 2023
- 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 |
More from HC Biologics, LLC
| 510(k) | Device | Decision |
|---|---|---|
| K251735 | Stabilis SA Cervical Stand-Alone System (Various PNs)OVE · Traditional | 07/30/2025SE |
| K251335 | Tera Lumbar Interbody Fusion System (Various PNs)MAX · Traditional | 06/02/2025SE |
| K243386 | Ventris Intervertebral Body Fusion DeviceOVD · Traditional | 04/22/2025SE |
| K241413 | sagAlign Lumbar Cage System (Various PNs)MAX · Traditional | 07/17/2024SE |
| K222561 | AlignOVD · Special | 09/23/2022SE |
| K221535 | Align Lumbar Interbody Fusion SystemMAX · Traditional | 07/22/2022SE |
| K201671 | A-Link ZOVD · Traditional | 05/04/2021SE |
Questions and answers
When was Align Cervical Interbody Fusion System cleared by the FDA?
Align Cervical Interbody Fusion System (K230639) received a 510(k) decision of Substantially Equivalent on December 1, 2023, 268 days after the submission was received.
What is the product code of K230639?
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.