PIONEER LABORATORIES BONE SCREW— 510(k) K940690

Name: FDA 510(k) clearance K940690
Creator: U.S. Food and Drug Administration
Published: 1994-11-22

Substantially Equivalent for Some Indications

Pioneer Surgical Technology

FDA 510(k) clearance K940690 for PIONEER LABORATORIES BONE SCREW, Substantially Equivalent for Some Indications on 1994-11-22. Applicant: Pioneer Surgical Technology. Device class: 2.

Clearance details

Applicant: Pioneer Surgical Technology
Product code: Code HWC
Device class: Class 2
Regulation: 21 CFR 888.3040
Advisory panel: Orthopedic
Date received: 1994-02-16
Decision date: 1994-11-22
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Marquette, MI, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code HWC

product code HWC

Death: 20
Injury: 15,910
Malfunction: 8,192
Other: 1
Total: 24,123

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.