# Mtp Solutions, LLC

- Location (FDA's records): Logan, UT
- FDA decisions: 4 (2014–2014): 4 510(k) clearances
- Product codes: MBI (2), HWC (2)
- Predicates its devices cite: 13 (1 its own); citations of its devices by later devices: 6 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Arthrex, Inc.: 10 (https://510kreport.com/company/arthrex)
- Osteomed LP: 1 (https://510kreport.com/company/osteomed)
- Nextremity Solutions, Inc.: 1 (https://510kreport.com/company/nextremity-solutions)

## Firms that cite its devices most
- Crossroads Extremity Systems, LLC: 2 (https://510kreport.com/company/crossroads-extremity-systems)
- Synchro Medical: 1 (https://510kreport.com/company/synchro-medical)
- Mortise Medical, LLC: 1 (https://510kreport.com/company/mortise-medical)
- Nextremity Solutions, Inc.: 1 (https://510kreport.com/company/nextremity-solutions)

## Its most-cited devices
- K133235: Threaded Peek K-Wire (2014), cited by 2
- K133229: Titanium Suture Anchor (2014), cited by 2
- K133515: Peek Fusion Implant (2014), cited by 2

## Recent decisions
- K140970: One-Piece Peek Fusion Implant (May 13, 2014)
- K133235: Threaded Peek K-Wire (Apr 7, 2014)
- K133515: Peek Fusion Implant (Mar 28, 2014)
- K133229: Titanium Suture Anchor (Jan 30, 2014)

Source page: https://510kreport.com/company/mtp-solutions