# K110473: Nanotack Suture Anchor 1.4MM

- Pathway: 510(k) (Traditional)
- Applicant: Pivot Medical
- Decided: May 25, 2011 after 96 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: 5 generations back to K961555 (1996). 38 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 41 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071586: Bioraptor 2.3 PK Suture Anchor, Smith & Nephew Inc., Endoscopy Division (2007) Summary page 1.
- K080088: Biomet Sports Medicine Anchor Devices and Ziploop Constructs, Biomet Manufacturing, Inc. (2008) Summary page 1.
- K101063: Sleeve with Ziploop Fixation Devices, Biomet Sports Medicine (2010) Summary page 1.

## Most influential descendants
- K130351: Nanotack Suture Anchor 1.4MM with Flex Inserter (2013), 0 descendants of its own
- K123651: Cinchlock Knotless Suture Anchor (2013), 0 descendants of its own

## Indications for use
The NanoTack Suture Anchor is indicated for the reattachment of hip labrum to the acetabulum.

Source page: https://510kreport.com/device/K110473
Methodology: https://510kreport.com/methodology