# Sagico VA USA, LLC

- Location (FDA's records): Tampa, FL
- FDA decisions: 3 (2023–2023): 3 510(k) clearances
- Product codes: OVE (2), NKB (1)
- 510(k) review time since 2016: median 265 days, against 97 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 10 (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
- Stryker Spine: 2 (https://510kreport.com/company/stryker-spine)
- Spinal Analytics & Geometrical Impant Co, LLC: 2 (https://510kreport.com/company/spinal-analytics-geometrical-impant)
- Spinal Analytics & Geometrical Implant Co, LLC: 1 (https://510kreport.com/company/spinal-analytics-geometrical-implant)
- Medtronic Sofamor Danek: 1 (https://510kreport.com/company/medtronic-sofamor-danek)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Materialise NV: 1 (https://510kreport.com/company/materialise)
- Ldr Spine USA: 1 (https://510kreport.com/company/ldr-spine-usa)
- Kalitec Direct, LLC: 1 (https://510kreport.com/company/kalitec-direct)

## Firms that cite its devices most
- Spinal Analytics & Geometrical Implant Co, LLC: 1 (https://510kreport.com/company/spinal-analytics-geometrical-implant)

## Its most-cited devices
- K221138: Titus Titanium Cervical by SAGICO (2023), cited by 1

## Recent decisions
- K232561: Ripley Spinal Screw System by SAGICO (Oct 23, 2023)
- K221138: Titus Titanium Cervical by SAGICO (Aug 4, 2023)
- K223143: SAGICO Spinal System (Jun 26, 2023)

Source page: https://510kreport.com/company/sagico-va-usa