Class Class II
JuggerKnot Soft Anchor (K231128)
Description
JuggerKnot Soft Anchor by Riverpoint Medical, LLC, an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK231128
Clearance Date2023-05-17
Clearance TypeSpecial
Product CodeMBI
Regulation Number888.3040
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K231128
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. JuggerKnot Soft Anchor (K231128) cites 1 predicate device and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K203740 | JuggerKnot Soft Anchor | Riverpoint Medical | 2021 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K240719 | OC JuggerKnot Soft Anchor | Riverpoint Medical | 2024 |
Trace the full predicate network for K231128
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.