FDA 510(k), K220131, KYPHON VuE Bone Cement
FDA 510(k), K220131, KYPHON VuE Bone Cement
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$149.00 USD
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$149.00 USD
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510(K) Number: K220131
Device Name: KYPHON VuE Bone Cement
Manufacturer: Massio Grazioli
Device Classification Name: Cement, Bone, Vertebroplasty
Regulation Number: NDN
Classification Product Code: 01/18/2022
Date Received: 04/18/2022
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
Device Name: KYPHON VuE Bone Cement
Manufacturer: Massio Grazioli
Device Classification Name: Cement, Bone, Vertebroplasty
Regulation Number: NDN
Classification Product Code: 01/18/2022
Date Received: 04/18/2022
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic