FDA 510(k), K141049, IFUSE IMPLANT SYSTEM
FDA 510(k), K141049, IFUSE IMPLANT SYSTEM
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$149.00 USD
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510(K) Number: K141049
Device Name: IFUSE IMPLANT SYSTEM
Manufacturer:
Device Classification Name: Sacroiliac Joint Fixation
Regulation Number: 888.3040
Classification Product Code: OUR
Date Received: 04/23/2014
Decision Date: 07/23/2014
Regulation Medical Specialty: Orthopedic
Device Name: IFUSE IMPLANT SYSTEM
Manufacturer:
Device Classification Name: Sacroiliac Joint Fixation
Regulation Number: 888.3040
Classification Product Code: OUR
Date Received: 04/23/2014
Decision Date: 07/23/2014
Regulation Medical Specialty: Orthopedic