DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM— 510(k) K980447
Substantially Equivalent for Some IndicationsDePuy Orthopaedics, Inc.
FDA 510(k) clearance K980447 for DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM, Substantially Equivalent for Some Indications on 1998-04-14. Applicant: DePuy Orthopaedics, Inc..
Clearance details
- Applicant
- DePuy Orthopaedics, Inc.
- Product code
- Code MNH
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent for Some Indications
- Clearance type
- Traditional
- Location
- Warsaw, IN, US
Adverse events under product code MNH
product code MNH- Injury
- 978
- Malfunction
- 793
- Total
- 1,771
Source: openFDA MAUDE database, through . 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.