STRYKER CROSSFLOW ARTHROSCOPY PUMP— 510(k) K123441

Substantially Equivalent

Stryker Endoscopy

FDA 510(k) clearance K123441 for STRYKER CROSSFLOW ARTHROSCOPY PUMP, Substantially Equivalent on 2013-01-09. Applicant: Stryker Endoscopy.

Clearance details

Applicant: Stryker Endoscopy
Product code: Code HRX
Advisory panel: Orthopedic
Date received: 2012-11-08
Decision date: 2013-01-09
Decision: Substantially Equivalent
Clearance type: Traditional
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.