Lanx Fusion System
FDA 510(k) K102738 · Lanx, LLC
510(k) numberK102738
Submission
- Device name
- Lanx Fusion System
- Applicant
- Lanx, LLC
Broomfield, CO, US - Received
- September 22, 2010
- Decision date
- February 10, 2011
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- OVD – Intervertebral Fusion Device With Integrated Fixation, Lumbar
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3080
- Specialty
- Orthopedic
- Implant
- Yes
Intended to stabilize lumbar spinal segment to promote fusion in order to restrict motion and decrease pain using bone graft with or without supplemental fixation.
Other 510(k)s with product code OVD
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K262025 | Innovasis AxTiHA® Stand-Alone ALIF System;Innovasis TxTiHA® IBF System;Innovasis…OVD · Traditional | INNO Holdings Inc. DBA Innovasis | 09/11/2026SE |
| K261408 | SABER-XA SystemOVD · Traditional | Elevation Spine | 08/03/2026SE |
| K261809 | Interwedge® Standalone LateralOVD · Special | Foundation Surgical Group | 07/31/2026SE |
| K261353 | Tesera-K Anterior Lumbar Interbody Fusion (ALIF) System; Tesera-K XL System; Lumbar…OVD · Traditional | Kyocera Medical Technologies, Inc. | 07/15/2026SE |
| K260810 | Anteralign LS coverplateOVD · Traditional | Tyber Medical, LLC | 06/10/2026SE |
| K254202 | MectaLIF 3D Metal AnteriorOVD · Traditional | Medacta International S.A. | 05/05/2026SE |
| K253401 | SCRIPT Implant SystemOVD · Traditional | Globus Medical, Inc. | 04/29/2026SE |
| K253559 | Ventana A Anterior Lumbar Interbody SystemOVD · Traditional | Spinal Elements, Inc. | 02/25/2026SE |
| K251829 | DeGen Medical Patient Specific Implant (PSI) SystemOVD · Traditional | Degen Medical | 12/08/2025SE |
| K251575 | IdentiTi II ALIF Standalone Interbody System; Transcend ALIF Standalone Interbody SystemOVD · Traditional | Alphatec Spine | 09/03/2025SE |
More from Alphatec Spine
| 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 Fusion System cleared by the FDA?
Lanx Fusion System (K102738) received a 510(k) decision of Substantially Equivalent on February 10, 2011, 141 days after the submission was received.
What is the product code of K102738?
The FDA product code is OVD – Intervertebral Fusion Device With Integrated Fixation, Lumbar, a Class II (moderate risk) device regulated under 21 CFR 888.3080.