Class Class II
Stryker AlphaVent™ Knotless SP Biocomposite Anchor (K250528)
Description
Stryker AlphaVent™ Knotless SP Biocomposite Anchor by Stryker Endoscopy, an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK250528
Clearance Date2025-05-21
Clearance TypeTraditional
Product CodeMAI
Regulation Number888.3030
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K250528
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. Stryker AlphaVent™ Knotless SP Biocomposite Anchor (K250528) cites 3 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K233893 | AlphaVent Knotless SP PEEK Anchor | Stryker Endoscopy | 2024 |
| K231093 | AlphaVent Suture Anchors | Stryker Endoscopy | 2023 |
| K203495 | Arthrex SwiveLock Anchor | Arthrex, Inc. | 2021 |
Trace the full predicate network for K250528
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.