Class Class II
Anika Tissue Tack Fixation System (K222487)
Description
Anika Tissue Tack Fixation System by Anika Therapeutics, Inc., an FDA 510(k) cleared general, plastic surgery device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK222487
Clearance Date2023-05-08
Clearance TypeTraditional
Product CodeGDW
Regulation Number878.4750
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K222487
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. Anika Tissue Tack Fixation System (K222487) cites 3 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K203117 | TissueTak device | Via Surgical , Ltd. | 2021 |
| K170278 | OptiFix AT Absorbable Fixation System with Articulating Tec... | C.R. Bard, Inc. | 2017 |
| K131637 | ROTATION MEDICAL SOFT TISSUE STAPLE (RMST STAPLE) | Rotation Medical, Inc. | 2013 |
Trace the full predicate network for K222487
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.