# K180361: MICRORAPTOR REGENESORB Suture Anchor

- Pathway: 510(k) (Traditional)
- Applicant: Smith and Nephew, Inc.
- Decided: May 30, 2018 after 110 days
- Product code: MAI (Fastener, Fixation, Biodegradable, Soft Tissue)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K961555 (1996). 15 ancestors in all.
4 later devices descend from it; 1 cites it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K101459: Osteoraptor II Suture Anchor or to BE Determined Model: 72202764 72202765 72202766 72202767 72202768 72202769 72202770, Smith & Nephew, Inc. (2011) Summary page 4.
- K082215: Osteoraptor Suture Anchor, Smith & Nephew Inc., Endoscopy Division (2008) Summary page 4.
- K131769: Cinchlock Knotless Suture Anchor, Nanotack Suture Anchor 1.4MM, Pivot Medical, Inc. (2013) Summary page 4.

## Most influential descendants
- K181746: MICRORAPTOR Knotless Suture Anchor (2018), 3 descendants of its own
- K251809: Arthrex FiberTak Suture Anchor (2025), 1 descendant of its own
- K260561: Arthrex FiberTak Suture Anchor (2026), 0 descendants of its own
- K252314: Arthrex SutureTak Suture Anchor (2025), 0 descendants of its own

## Indications for use
The Smith & Nephew MICRORAPTOR Suture Anchor is intended for the reattachment of soft tissue to bone for the following indications: Hip Acetabular labrum repair/reconstruction Shoulder • Capsular stabilization – Bankart repair – Anterior shoulder instability – SLAP lesion repairs – Capsular shift or capsulolabral reconstructions • Biceps tenodesis

Source page: https://510kreport.com/device/K180361
Methodology: https://510kreport.com/methodology