NBD CEMENT RESTRICTOR DEVICE— 510(k) K021788
UnknownNew Business Development, LLC
FDA 510(k) clearance K021788 for NBD CEMENT RESTRICTOR DEVICE, Unknown on 2002-10-04. Applicant: New Business Development, LLC.
Clearance details
- Applicant
- New Business Development, LLC
- Product code
- Code JDK
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Woodstock, GA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.