ACUSTAR I ADVANCED SURGICAL NAVIGATION SYSTEM— 510(k) K944612

Substantially Equivalent

Codman & Shurtleff, Inc.

FDA 510(k) clearance K944612 for ACUSTAR I ADVANCED SURGICAL NAVIGATION SYSTEM, Substantially Equivalent on 1995-12-11. Applicant: Codman & Shurtleff, Inc..

Clearance details

Applicant: Codman & Shurtleff, Inc.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 1994-09-19
Decision date: 1995-12-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raynham, MA, US

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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.