# Frontier Medical Devices, Inc.

- Location (FDA's records): Gwinn, MI
- FDA decisions: 5 (2012–2016): 5 510(k) clearances
- Product codes: JDQ (3), OVD (2)
- Predicates its devices cite: 14 (2 its own); citations of its devices by later devices: 2 (2 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
- Pioneer Surgical Technology: 8 (https://510kreport.com/company/pioneer-surgical-technology)
- Nuvasive, Inc.: 1 (https://510kreport.com/company/nuvasive)
- Medtronic Sofamor Danek: 1 (https://510kreport.com/company/medtronic-sofamor-danek)
- Nu Vasive, Incorporated: 1 (https://510kreport.com/company/nu-vasive)
- Zimmer Spine, Inc.: 1 (https://510kreport.com/company/zimmer-spine)

## Its most-cited devices
- K112700: Frontier Sadl Interbody Fusion Device (2012), cited by 1
- K151888: Frontier Medical Devices In-line Orthopedic Cable Cerclage System (2015), cited by 1

## Recent decisions
- K153242: Frontier Medical Devices In-Line Orthopedic Cable Cerclage System (Jan 13, 2016)
- K151888: Frontier Medical Devices In-line Orthopedic Cable Cerclage System (Oct 30, 2015)
- K151346: Frontier Medical Devices Posterior Cable Screw System (Aug 20, 2015)
- K143228: Ancora LLC Interbody Fusion Device (Feb 26, 2015)
- K112700: Frontier Sadl Interbody Fusion Device (Nov 1, 2012)

Source page: https://510kreport.com/company/frontier-medical-devices