WRIGHT PLASTER OF PARIS PELLETS (SUBJECT TO REVISION)— 510(k) K960978

Substantially Equivalent

Wrightmedicaltechnologyinc

FDA 510(k) clearance K960978 for WRIGHT PLASTER OF PARIS PELLETS (SUBJECT TO REVISION), Substantially Equivalent on 1996-06-21. Applicant: Wrightmedicaltechnologyinc.

Clearance details

Applicant: Wrightmedicaltechnologyinc
Product code: Code MQV
Advisory panel: Orthopedic
Date received: 1996-03-11
Decision date: 1996-06-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington, TN, US

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Adverse events under product code MQV

product code MQV

Death: 6
Injury: 435
Total: 441

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.