# Medtronic-Synectics

- Location (FDA's records): Stockholm, SE
- FDA decisions: 1 (1997–1997): 1 510(k) clearance
- Product codes: FFX (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 1 (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
- Synectics-Dantec: 1 (https://510kreport.com/company/synectics-dantec)

## Firms that cite its devices most
- Medtronic Functional Diagnostics A/S: 1 (https://510kreport.com/company/medtronic-functional-diagnostics-a-s)

## Its most-cited devices
- K972439: Anorectal Manometry Analysis Module (1997), cited by 1

## Recent decisions
- K972439: Anorectal Manometry Analysis Module (Sep 23, 1997)

Source page: https://510kreport.com/company/medtronic-synectics