CROSSNAV Navigation Enabled Instruments and UNAS Navigation Arrays (K241893)
Description
CROSSNAV Navigation Enabled Instruments and UNAS Navigation Arrays by Medos International SARL, an FDA 510(k) cleared neurology device.
Regulatory Information
FDA Database
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Predicate lineage for K241893
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. CROSSNAV Navigation Enabled Instruments and UNAS Navigation Arrays (K241893) cites 4 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K233255 | CROSSNAV Navigation Enabled Instruments | DePuy Synthes | 2024 |
| K233254 | TELIGEN System Navigation Ready Instruments | DePuy Synthes | 2024 |
| K221618 | Spine & Trauma Navigation, Spine Navigation, Navigation Sof... | Brainlab AG | 2022 |
| K201661 | Symphony Navigation Ready Instruments and Universal Navigat... | Medos International SARL | 2020 |
Trace the full predicate network for K241893
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.