# Biomet Micofixation

- Location (FDA's records): Jacksonville, FL
- FDA decisions: 3 (2021–2022): 3 510(k) clearances
- Product codes: HRS (2), HBE (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 5 (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
- Walter Lorenz Surgical, Inc.: 2 (https://510kreport.com/company/walter-lorenz-surgical)
- Sig Medical Corp.: 1 (https://510kreport.com/company/sig-medical)

## Firms that cite its devices most
- Biomet Microfixation: 2 (https://510kreport.com/company/biomet-microfixation)
- Riverpoint Medical: 1 (https://510kreport.com/company/riverpoint-medical)
- Costa Surgical, Inc.: 1 (https://510kreport.com/company/costa-surgical)
- Chest Wall Innovations, Inc.: 1 (https://510kreport.com/company/chest-wall-innovations)

## Its most-cited devices
- K203474: Biomet Microfixation RibFix Advantage System (2021), cited by 3
- K213072: 2.1 x 255mm Drill, 22mm Stop (2022), cited by 1
- K212841: Pectus Blu Support Bar System (2022), cited by 1

## Recent decisions
- K213072: 2.1 x 255mm Drill, 22mm Stop (Aug 23, 2022)
- K212841: Pectus Blu Support Bar System (Jan 7, 2022)
- K203474: Biomet Microfixation RibFix Advantage System (Jan 28, 2021)

Source page: https://510kreport.com/company/biomet-micofixation