# Neos Surgery S.L

- Location (FDA's records): Barcelona, ES
- FDA decisions: 6 (2010–2024): 6 510(k) clearances
- Product codes: GXR (4), JDQ (2)
- Predicates its devices cite: 10 (4 its own); citations of its devices by later devices: 6 (4 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
- Aesculap, Inc.: 2 (https://510kreport.com/company/aesculap)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Howmedica Corp.: 1 (https://510kreport.com/company/howmedica)
- NeuroPace, Inc.: 1 (https://510kreport.com/company/neuropace)
- Medtronic PS Medical: 1 (https://510kreport.com/company/medtronic-ps-medical)

## Firms that cite its devices most
- Ossaware Biotech Co., Ltd.: 2 (https://510kreport.com/company/ossaware-biotech)

## Its most-cited devices
- K132044: Cranial Loop, Cranial Loop L and Cranial Loop XL and Cranial Bone Fixation System (2013), cited by 3
- K211613: Stern Fix Sternal Stabilization System (2022), cited by 1
- K160739: Cranial COVER (2016), cited by 1
- K101235: Cranial Loop Cranial Bone Fixation System (2010), cited by 1

## Recent decisions
- K240137: Cranial LOOP, Cranial LOOP L and Cranial LOOP XL Cranial Bone Fixation System (Feb 16, 2024)
- K221795: STERN FIX Sternal Stabilization System (Oct 19, 2022)
- K211613: Stern Fix Sternal Stabilization System (Jan 19, 2022)
- K160739: Cranial COVER (Jun 12, 2016)
- K132044: Cranial Loop, Cranial Loop L and Cranial Loop XL and Cranial Bone Fixation System (Sep 30, 2013)
- K101235: Cranial Loop Cranial Bone Fixation System (Oct 25, 2010)

Source page: https://510kreport.com/company/neos-surgery-s-l