Lanx Cervical Intervertebral Body Fusion System
FDA 510(k) K103660 · Lanx, Inc.
510(k) numberK103660
Submission
- Device name
- Lanx Cervical Intervertebral Body Fusion System
- Applicant
- Lanx, Inc.
Broomfield, CO, US - Received
- December 15, 2010
- Decision date
- February 28, 2011
- 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 |
|---|---|---|
| K131547 | Lanx Fusion SystemOVD · Special | 07/12/2013SE |
| K131156 | Lanx Spinal Fixation SystemKWP · Special | 05/24/2013SE |
| K123767 | Lanx Fusion System- SAOVD · Traditional | 03/18/2013SE |
| K121316 | Lanx Spinal Fization SystemNKB · Traditional | 09/10/2012SE |
| K122145 | Lanx Spinal Fixation SystemNKB · Special | 08/17/2012SE |
| K121940 | Lanx Spinal Fixation SystemNKB · Special | 08/02/2012SE |
| K120399 | Lanx Spinal Fixation SystemNKB · Special | 03/09/2012SE |
| K113434 | Lanx Posterior Cervicothoracic Spinal Fixation System (PCFS)NKB · Special | 12/19/2011SE |
| K112388 | Lanx Cervical SAOVE · Traditional | 12/16/2011SE |
| K103091 | Lanx Spinal Fixation SystemKWP · Special | 04/15/2011SE |
Questions and answers
When was Lanx Cervical Intervertebral Body Fusion System cleared by the FDA?
Lanx Cervical Intervertebral Body Fusion System (K103660) received a 510(k) decision of Substantially Equivalent on February 28, 2011, 75 days after the submission was received.
What is the product code of K103660?
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.