uCerv Flux-C 3D Porous Titanium Cervical Interbody
FDA 510(k) K241396 · Ulrich Medical USA, Inc.
510(k) numberK241396
Submission
- Device name
- uCerv Flux-C 3D Porous Titanium Cervical Interbody
- Applicant
- Ulrich Medical USA, Inc.
Plano, TX, US - Received
- May 16, 2024
- Decision date
- May 23, 2024
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 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 |
|---|---|---|
| K252087 | Navigation Module of the Cortium® SystemOLO · Traditional | 02/03/2026SE |
| K251719 | Momentum® Posterior Spinal Fixation SystemNKB · Special | 07/01/2025SE |
| K240515 | uNion® MAX Cervical Plate SystemKWQ · Special | 03/18/2024SE |
| K231809 | Momentum® Posterior Spinal Fixation System with G21 V-STEADY Bone Cement; Momentum® MIS…PML · Traditional | 10/20/2023SE |
| K230614 | CortiumNKG · Traditional | 05/02/2023SE |
| K223274 | Momentum® MIS Posterior Spinal Fixation SystemNKB · Special | 11/28/2022SE |
| K220696 | uCerv Flux-C 3D Porous Titanium Cervical InterbodyODP · Traditional | 08/19/2022SE |
| K200845 | Navigation Module of the Momentum SystemOLO · Traditional | 09/10/2020SE |
| K191932 | Momentum Posterior Spinal Fixation SystemNKB · Traditional | 10/02/2019SE |
| K181921 | Solidity Vertebral Body ReplacementMQP · Traditional | 11/16/2018SE |
Questions and answers
When was uCerv Flux-C 3D Porous Titanium Cervical Interbody cleared by the FDA?
uCerv Flux-C 3D Porous Titanium Cervical Interbody (K241396) received a 510(k) decision of Substantially Equivalent on May 23, 2024, 7 days after the submission was received.
What is the product code of K241396?
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.