# Cmf Medicon Surgical, Inc.

- Location (FDA's records): Jacksonville, FL
- FDA decisions: 4 (2019–2024): 4 510(k) clearances
- Product codes: NKB (1), PLR (1), FZE (1), MQP (1)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 0 (0 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
- Astura Medical: 1 (https://510kreport.com/company/astura-medical)
- Spineart: 1 (https://510kreport.com/company/spineart)
- Nu Vasive, Incorporated: 1 (https://510kreport.com/company/nu-vasive)
- Aesculap Implants Systems, LLC: 1 (https://510kreport.com/company/aesculap-implants-systems)
- Southern Implants (Pty), Ltd.: 1 (https://510kreport.com/company/southern-implants)
- Nuvasive, Inc.: 1 (https://510kreport.com/company/nuvasive)
- Aesculap Implant System, Inc.: 1 (https://510kreport.com/company/aesculap-implant-system)

## Recent decisions
- K241253: Medicon Epiplating System (Dec 12, 2024)
- K242764: MediRod Pedicle Screw System (Nov 13, 2024)
- K212126: MediExpand Cervical Expandable VBR System (Apr 4, 2022)
- K190349: MediExpand TL Expandable VBR System (Oct 24, 2019)

Source page: https://510kreport.com/company/cmf-medicon-surgical