OSCILLATING BONE SAW BLADE, 6200 SERIES— 510(k) K934390

Substantially Equivalent

Boehringer Laboratories

FDA 510(k) clearance K934390 for OSCILLATING BONE SAW BLADE, 6200 SERIES, Substantially Equivalent on 1994-01-26. Applicant: Boehringer Laboratories.

Clearance details

Applicant: Boehringer Laboratories
Product code: Code GFA
Advisory panel: General, Plastic Surgery
Date received: 1993-09-09
Decision date: 1994-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norristown, PA, US

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Adverse events under product code GFA

product code GFA

Death: 2
Injury: 140
Malfunction: 2,337
Total: 2,479

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.