IMPLANT LOCATION SOFTWARE, MODEL 0.1.0— 510(k) K050341

Substantially Equivalent

Tactile Technologies, Ltd.

FDA 510(k) clearance K050341 for IMPLANT LOCATION SOFTWARE, MODEL 0.1.0, Substantially Equivalent on 2005-03-29. Applicant: Tactile Technologies, Ltd..

Clearance details

Applicant: Tactile Technologies, Ltd.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2005-02-11
Decision date: 2005-03-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rechovot, IL

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Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

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.