Class Class II
Osprey Suture Anchor (K243726)
Description
Osprey Suture Anchor by Responsive Arthroscopy, Inc., an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK243726
Clearance Date2025-01-30
Clearance TypeTraditional
Product CodeMBI
Regulation Number888.3040
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K243726
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. Osprey Suture Anchor (K243726) cites 3 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K180951 | Responsive Arthroscopy Suture Anchor System | Responsive Arthroscopy, LLC | 2019 |
| K173845 | Arthrex SwiveLock | Arthrex, Inc. | 2018 |
| K173485 | Amsco Evolution Medium Steam Sterilizer | STERIS Corporation | 2018 |
Trace the full predicate network for K243726
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.