# K160118: STROPP (Single Tunnel Repair of Plantar Plate)

- Pathway: 510(k) (Traditional)
- Applicant: Crossroads Extremity Systems, LLC
- Decided: May 3, 2016 after 105 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: 8 generations back to K961555 (1996). 16 ancestors in all.
No later device cites it as a predicate yet.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K133229: Titanium Suture Anchor, Mtp Solutions, LLC (2014) Summary page 4.
- K133235: Threaded Peek K-Wire, Mtp Solutions, LLC (2014) Summary page 4.

## Indications for use
The STROPP(TM) System is intended for use with a suture in metatarsal ligament and tendon repairs.

Source page: https://510kreport.com/device/K160118
Methodology: https://510kreport.com/methodology