Ancora LLC Interbody Fusion Device
FDA 510(k) K143228 · Frontier Medical Devices, Inc.
510(k) numberK143228
Submission
- Device name
- Ancora LLC Interbody Fusion Device
- Applicant
- Frontier Medical Devices, Inc.
Gwinn, MI, US - Received
- November 10, 2014
- Decision date
- February 26, 2015
- 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
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|---|---|---|---|
| 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 |
|---|---|---|
| K153242 | Frontier Medical Devices In-Line Orthopedic Cable Cerclage SystemJDQ · Traditional | 01/13/2016SE |
| K151888 | Frontier Medical Devices In-line Orthopedic Cable Cerclage SystemJDQ · Traditional | 10/30/2015SE |
| K151346 | Frontier Medical Devices Posterior Cable Screw SystemJDQ · Traditional | 08/20/2015SE |
| K112700 | Frontier Sadl Interbody Fusion DeviceOVD · Traditional | 11/01/2012SE |
Questions and answers
When was Ancora LLC Interbody Fusion Device cleared by the FDA?
Ancora LLC Interbody Fusion Device (K143228) received a 510(k) decision of Substantially Equivalent on February 26, 2015, 108 days after the submission was received.
What is the product code of K143228?
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.