FDA 510(k), K123909, AESCULAP CESPACE XP
FDA 510(k), K123909, AESCULAP CESPACE XP
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$149.00 USD
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510(K) Number: K123909
Device Name: AESCULAP CESPACE XP
Manufacturer:
Device Classification Name: Intervertebral Fusion Device With Bone Graft, Cervical
Regulation Number: 888.3080
Classification Product Code: ODP
Date Received: 12/19/2012
Decision Date: 04/15/2013
Regulation Medical Specialty: Orthopedic
Device Name: AESCULAP CESPACE XP
Manufacturer:
Device Classification Name: Intervertebral Fusion Device With Bone Graft, Cervical
Regulation Number: 888.3080
Classification Product Code: ODP
Date Received: 12/19/2012
Decision Date: 04/15/2013
Regulation Medical Specialty: Orthopedic