Turbett Instrument Pod— 510(k) K200240

Substantially Equivalent

Turbett Surgical, Inc.

FDA 510(k) clearance K200240 for Turbett Instrument Pod, Substantially Equivalent on 2020-04-30. Applicant: Turbett Surgical, Inc..

Clearance details

Applicant: Turbett Surgical, Inc.
Product code: Code FRG
Advisory panel: General Hospital
Date received: 2020-01-31
Decision date: 2020-04-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FRG

product code FRG

Other: 3
Total: 3

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.