BK220700 - SMARTGRAFT 30 SYSTEM
510(k) Number: BK220700
Applicant: INGENERON INC.
Device Name: SMARTGRAFT 30 SYSTEM
Decision Date: 9/24/2014
On Oct. 1, 2024, the FDA began implementing a reorganization impacting many parts of the agency. We are in the process of updating FDA.gov content to reflect these changes.
510(k) Number: BK220700
Applicant: INGENERON INC.
Device Name: SMARTGRAFT 30 SYSTEM
Decision Date: 9/24/2014