Class Class II
VersaCross™ RF Wire (K242076)
Description
VersaCross™ RF Wire by Baylis Medical Company, an FDA 510(k) cleared cardiovascular device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242076
Clearance Date2024-11-01
Clearance TypeSpecial
Product CodeDXF
Regulation Number870.5175
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242076
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. VersaCross™ RF Wire (K242076) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K150709 | ProTrack RF Anchor Wire | Baylis Medical Company, Inc. | 2015 |
Trace the full predicate network for K242076
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.