DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM - PEDICLE FIXATION— 510(k) K950697

Substantially Equivalent

Depuy Motech

FDA 510(k) clearance K950697 for DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM - PEDICLE FIXATION, Substantially Equivalent on 1995-06-22. Applicant: Depuy Motech.

Clearance details

Applicant: Depuy Motech
Product code: Code MNH
Advisory panel: Orthopedic
Date received: 1995-02-06
Decision date: 1995-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Warsaw, IN, US

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Adverse events under product code MNH

product code MNH

Injury: 978
Malfunction: 793
Total: 1,771

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.