# K061154: Kinsa Suture Anchor

- Pathway: 510(k) (Traditional)
- Applicant: Smith & Nephew, Inc.
- Decided: Jun 8, 2006 after 43 days
- Product code: MBI (Fastener, Fixation, Nondegradable, Soft Tissue)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K961555 (1996). 4 ancestors in all.
162 later devices descend from it; 3 cite it directly.
0 of 167 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K053344: Bioraptor Suture Anchor, Twinfix 2.8 MM Suture Anchor, Twinfix 3.5 MM Suture Anchor, Smith & Nephew, Inc. (2006) Summary page 1.

## Most influential descendants
- K071586: Bioraptor 2.3 PK Suture Anchor (2007), 121 descendants of its own
- K070908: Smith & Nephew Kinsa RC Suture Anchor (2007), 60 descendants of its own
- K072785: Twinfix FT PK (2007), 59 descendants of its own
- K082215: Osteoraptor Suture Anchor (2008), 46 descendants of its own
- K093428: Smith & Nephew Knotless Instability Anchor (2009), 41 descendants of its own

## Indications for use
The Smith & Nephew KINSA Suture Anchor is intended for use for the reattachment of soft tissue to bone for the following indications: Shoulder Capsular Stabilization Bankhart Repair Anterior Shoulder Instability Repair SLAP Lesion Repairs Capsular Shift of capsulolabral reconstructions Acromioclavicular separation repairs Deltoid Repairs Rotator Cuff Tear repairs Biceps tenodesis

Source page: https://510kreport.com/device/K061154
Methodology: https://510kreport.com/methodology