KLS Martin IPS Distraction— 510(k) K220050
Substantially EquivalentKLS Martin L.P.
FDA 510(k) clearance K220050 for KLS Martin IPS Distraction, Substantially Equivalent on 2022-08-11. Applicant: KLS Martin L.P..
Clearance details
- Applicant
- KLS Martin L.P.
- Product code
- Code MQN
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Jacksonville, FL, US
Adverse events under product code MQN
product code MQN- Injury
- 346
- Total
- 346
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.