BONE CURETTE— 510(k) K890252
Substantially EquivalentKinetic Medical Products
FDA 510(k) clearance K890252 for BONE CURETTE, Substantially Equivalent on 1989-01-27. Applicant: Kinetic Medical Products.
Clearance details
- Applicant
- Kinetic Medical Products
- Product code
- Code HTF
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Erie, PA, US
Adverse events under product code HTF
product code HTF- Other
- 1
- Total
- 1
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.