# K120356: NCS Fish-Fit MD System Fish-Fit MD Compass MD

- Pathway: 510(k) (Traditional)
- Applicant: Ncs Lab Srl
- Decided: Dec 11, 2012 after 309 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: 10 generations back to K911837 (1991). 85 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 87 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K100159: Smith and Nephew Twinfix Ultra TI Suture Anchor, Smith & Nephew Inc., Endoscopy Div. (2010) Summary page 2.
- K111779: Y-Knot All-Suture Anchor Model HF13, Conmed Linvatec (2011) Summary page 2.

## Most influential descendants
- K160500: Elite SPK, Compasso, Elite SPK Kit (2016), 0 descendants of its own

## Indications for use
The NCS Fish-Fit MID System is intended for the attachment of soft tissue to bone during arthroscopic or open treatment of rotator cuff tendons lesions with the purpose of repairing the rotator cuff (supraspinatus, infraspinatus and subscapularis).

Source page: https://510kreport.com/device/K120356
Methodology: https://510kreport.com/methodology