# Sutter Biomedical, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 11 (1981–1988): 11 510(k) clearances
- Product codes: BXB (4), KWD (2), MDM (1), KWH (1), JFA (1), KYJ (1), JDI (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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 that cite its devices most
- Avanta Orthopaedics, Inc.: 1 (https://510kreport.com/company/avanta-orthopaedics)
- Brm Extremities: 1 (https://510kreport.com/company/brm-extremities)
- Nexa Orthopedics, Inc.: 1 (https://510kreport.com/company/nexa-orthopedics)

## Its most-cited devices
- K870200: Sutter Finger Joint Prosthesis (1987), cited by 2
- K820813: Lesser Metatarsal Phalang. Joint Prosth (1982), cited by 1

## Recent decisions
- K875249: Sutter Phalangeal Cap (Feb 3, 1988)
- K870200: Sutter Finger Joint Prosthesis (Oct 9, 1987)
- K861983: Sutter Lesser Metatarsal Cap (Sep 8, 1986)
- K850274: Sutter CPM 9000 -Nonmeasuring Exercise Equipment (Apr 25, 1985)
- K830974: Sutter CPM 5000 (Apr 12, 1983)
- K830649: Sutter CPM 2000 (Mar 17, 1983)
- K823539: Sutter CPM (Jan 14, 1983)
- K820813: Lesser Metatarsal Phalang. Joint Prosth (May 21, 1982)

Source page: https://510kreport.com/company/sutter-biomedical