Class Class II
Citrepore™ (K240450)
Description
Citrepore™ by Acuitive Technologies, Inc., an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK240450
Clearance Date2024-11-06
Clearance TypeTraditional
Product CodeMQV
Regulation Number888.3045
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K240450
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. Citrepore™ (K240450) cites 5 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K232592 | CITRELOCK® DUO | Acuitive Technologies, Inc. | 2023 |
| K221468 | Citregen Tendon Interference Screw (TIS), Citrelock Tendo... | Acuitive Technologies, Inc. | 2023 |
| K210239 | CITRESPLINE and CITRELOCK ACL Implants | Acuitive Technologies, Inc. | 2021 |
| K200725 | Citregen Tendon Interference Screw and Citrelock | Acuitive Technologies | 2020 |
| K083033 | VITOSS BONE GRAFT SUBSTITUTE, BONE GRAFT SUBSTITUTE FILLED ... | Orthovita, Inc. | 2008 |
Trace the full predicate network for K240450
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.