Infill Cervical
FDA 510(k) K140066 · Pinnacle Spine Group, LLC
510(k) numberK140066
Submission
- Device name
- Infill Cervical
- Applicant
- Pinnacle Spine Group, LLC
Dallas, TX, US - Received
- January 10, 2014
- Decision date
- May 5, 2014
- 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 |
|---|---|---|
| K172349 | InFill® Interbody Fusion DeviceMAX · Traditional | 12/14/2017SE |
| K152259 | InFill Interbody Fusion DeviceMAX · Traditional | 11/19/2015SE |
| K151184 | InFill Interbody Fusion DevicesMAX · Traditional | 07/14/2015SE |
| K150206 | InFill Interbody Fusion DevicesMAX · Special | 04/03/2015SE |
| K143488 | InFill Graft Delivery SystemFMF · Special | 12/17/2014SE |
| K141282 | PGS 5.5 MM Cannulated Pedicle ScrewNKB · Traditional | 12/02/2014SE |
| K133721 | Infill 41-TLIF Convex Oblique Device, Infill 43-TLIF Contour Oblique, Infill 44-TLIF…MAX · Traditional | 03/31/2014SE |
| K124012 | Infill Oblique Tlif DeviceMAX · Traditional | 06/04/2013SE |
| K121476 | Infill Graft Delivery SystemFMF · Special | 08/29/2012SE |
| K121733 | Infill Intervertebral Body Fusion DeviceMAX · Special | 07/13/2012SE |
Questions and answers
When was Infill Cervical cleared by the FDA?
Infill Cervical (K140066) received a 510(k) decision of Substantially Equivalent on May 5, 2014, 115 days after the submission was received.
What is the product code of K140066?
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.