Stryker Consolidated Operating Room Equipment (CORE) 2 Console— 510(k) K171840
Substantially EquivalentStryker Corporation
FDA 510(k) clearance K171840 for Stryker Consolidated Operating Room Equipment (CORE) 2 Console, Substantially Equivalent on 2017-09-15. Applicant: Stryker Corporation.
Clearance details
- Applicant
- Stryker Corporation
- Product code
- Code ERL
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Kalamazoo, MI, US
Adverse events under product code ERL
product code ERL- Malfunction
- 11,234
- Total
- 11,234
Source: openFDA MAUDE database, through . 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.