DYONICS ARTHROSCOPIC KIT— 510(k) K920267

Unknown

Smith & Nephew Dyonics, Inc.

FDA 510(k) clearance K920267 for DYONICS ARTHROSCOPIC KIT, Unknown on 1993-03-23. Applicant: Smith & Nephew Dyonics, Inc..

Clearance details

Applicant: Smith & Nephew Dyonics, Inc.
Product code: Code LRO
Advisory panel: General, Plastic Surgery
Date received: 1992-01-21
Decision date: 1993-03-23
Decision: Unknown
Clearance type: Traditional
Location: Andover, MA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code LRO

product code LRO

Injury: 975
Malfunction: 14,038
Other: 2
Total: 15,015

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.