Reliance Lumbar IBF System— 510(k) K183049
Substantially EquivalentReliance Medical Systems, LLC
FDA 510(k) clearance K183049 for Reliance Lumbar IBF System, Substantially Equivalent on 2019-02-15. Applicant: Reliance Medical Systems, LLC.
Clearance details
- Applicant
- Reliance Medical Systems, LLC
- Product code
- Code MAX
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Bountiful, UT, US
Adverse events under product code MAX
product code MAX- Death
- 13
- Injury
- 1,305
- Malfunction
- 2,885
- Total
- 4,203
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.