CONDUIT™ Lateral Lumbar Intervertebral Fusion Cage, CONDUIT™ Instruments (K223688)
Description
CONDUIT™ Lateral Lumbar Intervertebral Fusion Cage, CONDUIT™ Instruments by Medos International Sàrl, an FDA 510(k) cleared orthopedic device.
Regulatory Information
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K223688
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. CONDUIT™ Lateral Lumbar Intervertebral Fusion Cage, CONDUIT™ Instruments (K223688) cites 7 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K222276 | CONDUIT Cages; FIBERGRAFT BG Putty | Depuy Spine | 2022 |
| K221325 | CONDUIT Lateral Switch Plate | Medos International SARL | 2022 |
| K203714 | NuVasive Thoracolumbar Interbody Systems: NuVasive CoRoent ... | Nu Vasive, Incorporated | 2021 |
| K210728 | CONDUIT Instruments | Medos International SARL | 2021 |
| K201605 | EIT Cellular Titanium Cervical Cage, EIT Cellular Titanium ... | Eit Emerging Implant Technologies GmbH | 2020 |
| K181644 | EIT Cellular Titanium® Lumbar Cage LLIF | Eit Emerging Implant Technologies GmbH | 2018 |
| K162358 | T-PAL Spacer System, T-PAL Titanium Spacer System, SYNFIX E... | Synthes USA Products, LLC | 2016 |
Trace the full predicate network for K223688
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.