Stryker Arthroscope— 510(k) K202659

Substantially Equivalent

Stryker

FDA 510(k) clearance K202659 for Stryker Arthroscope, Substantially Equivalent on 2020-12-01. Applicant: Stryker.

Clearance details

Applicant: Stryker
Product code: Code HRX
Advisory panel: Orthopedic
Date received: 2020-09-14
Decision date: 2020-12-01
Decision: Substantially Equivalent
Clearance type: Special
Location: San Jose, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code HRX

product code HRX

Injury: 623
Malfunction: 11,257
Total: 11,880

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.