ADG INTRAMEDULLARY BONE PLUG - VENTED— 510(k) K911717
Substantially EquivalentAmerican Design Group, Inc.
FDA 510(k) clearance K911717 for ADG INTRAMEDULLARY BONE PLUG - VENTED, Substantially Equivalent on 1991-09-04. Applicant: American Design Group, Inc..
Clearance details
- Applicant
- American Design Group, Inc.
- Product code
- Code LZN
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Concord, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.