SPINE-TECH BONE HARVESTER— 510(k) K970040

Name: FDA 510(k) clearance K970040
Creator: U.S. Food and Drug Administration
Published: 1997-02-28

Substantially Equivalent

Spine-Tech, Inc.

FDA 510(k) clearance K970040 for SPINE-TECH BONE HARVESTER, Substantially Equivalent on 1997-02-28. Applicant: Spine-Tech, Inc.. Device class: 1.

Clearance details

Applicant: Spine-Tech, Inc.
Product code: Code HWE
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1997-01-06
Decision date: 1997-02-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code HWE

product code HWE

Death: 4
Injury: 448
Malfunction: 19,856
Other: 2
Total: 20,310

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.