BONE MARROW BIOPSY SYSTEM— 510(k) K923872

Substantially Equivalent

The Straumann Co.

FDA 510(k) clearance K923872 for BONE MARROW BIOPSY SYSTEM, Substantially Equivalent on 1992-12-15. Applicant: The Straumann Co..

Clearance details

Applicant: The Straumann Co.
Product code: Code GDM
Advisory panel: General, Plastic Surgery
Date received: 1992-08-03
Decision date: 1992-12-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cambridge, MA, US

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Adverse events under product code GDM

product code GDM

Death: 2
Total: 2

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.