STEALTHSTATION SYSTEM— 510(k) K983670

Name: FDA 510(k) clearance K983670
Creator: U.S. Food and Drug Administration
Published: 1999-01-14

Substantially Equivalent

Surgical Navigation Technologies, Inc.

FDA 510(k) clearance K983670 for STEALTHSTATION SYSTEM, Substantially Equivalent on 1999-01-14. Applicant: Surgical Navigation Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Surgical Navigation Technologies, Inc.
Product code: Code HAW
Device class: Class 2
Regulation: 21 CFR 882.4560
Advisory panel: Neurology
Date received: 1998-10-19
Decision date: 1999-01-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Broomfield, CO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HAW

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K253856 — Geniant Cranial (Navigated Neurosurgical Positioning Robot)2026-09-10
K261932 — Leksell® Vantage Stereotactic System2026-08-05
K253663 — Zeta Navigation System2026-05-01
K253379 — Stealth AXiS Cranial clinical application2026-03-26
K231897 — NeuroAlign software2025-10-21

More clearances from Surgical Navigation Technologies, Inc.

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K000246 — RADIOCAMERAS EXTRACRANIAL SYSTEM2000-10-20
K994355 — RADIOCAMERAS SYSTEM HEAD/NECK APPLICATION2000-03-22
K992461 — STEALTHSTATION TREATMENT GUIDANCE PLATFORM2000-02-22
K992927 — STEALTHSTATION TREATMENT GUIDANCE PLATFORM1999-12-29
K993021 — METRX SYSTEM1999-11-10

Adverse events under product code HAW

product code HAW

Death: 52
Injury: 1,083
Malfunction: 17,300
Total: 18,435

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.