SUTTER FINGER JOINT PROSTHESIS— 510(k) K870200

Substantially Equivalent

Sutter Biomedical, Inc.

FDA 510(k) clearance K870200 for SUTTER FINGER JOINT PROSTHESIS, Substantially Equivalent on 1987-10-09. Applicant: Sutter Biomedical, Inc..

Clearance details

Applicant: Sutter Biomedical, Inc.
Product code: Code KYJ
Advisory panel: Orthopedic
Date received: 1987-01-20
Decision date: 1987-10-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KYJ

product code KYJ

Injury: 210
Total: 210

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.