PERCUDISC PLDD DELIVERY SYSTEM/PROCEDURE KIT— 510(k) K920673

Unknown

Percudisc, Inc.

FDA 510(k) clearance K920673 for PERCUDISC PLDD DELIVERY SYSTEM/PROCEDURE KIT, Unknown on 1992-08-13. Applicant: Percudisc, Inc..

Clearance details

Applicant: Percudisc, Inc.
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 1992-02-14
Decision date: 1992-08-13
Decision: Unknown
Clearance type: Traditional
Location: Mountain View, CA, US

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Adverse events under product code GEX

product code GEX

Death: 33
Injury: 3,045
Malfunction: 12,903
Other: 25
Total: 16,006

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.