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. Device class: 2.
Clearance details
- Applicant
- New Business Development, LLC
- Product code
- Code JDK
- Device class
- Class 2
- Regulation
- 21 CFR 878.3300
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Woodstock, GA, US
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