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FDA 510(k), K142095, RENOVIS S134 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM
FDA 510(k), K142095, RENOVIS S134 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM
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$149.00 USD
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$149.00 USD
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510(K) Number: K142095
Device Name: RENOVIS S134 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM
Manufacturer:
Device Classification Name: Intervertebral Fusion Device With Integrated Fixation, Lumbar
Regulation Number: 888.3080
Classification Product Code: OVD
Date Received: 08/01/2014
Decision Date: 10/15/2014
Regulation Medical Specialty: Orthopedic
Device Name: RENOVIS S134 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM
Manufacturer:
Device Classification Name: Intervertebral Fusion Device With Integrated Fixation, Lumbar
Regulation Number: 888.3080
Classification Product Code: OVD
Date Received: 08/01/2014
Decision Date: 10/15/2014
Regulation Medical Specialty: Orthopedic
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