FDA 510(k) Application Details - K193075

Device Classification Name Filler, Bone Void, Calcium Compound

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510(K) Number K193075
Device Name Filler, Bone Void, Calcium Compound
Applicant Sirakoss Ltd.
Level 4, Polwarth Building, Foresterhill
Aberdeen ab25 2zd GB
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Contact Jordan Conway
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Regulation Number 888.3045

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Classification Product Code MQV
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Date Received 11/04/2019
Decision Date 06/09/2020
Decision SESE - SUBST EQUIV
Classification Advisory Committee OR - Orthopedic
Review Advisory Committee OR - Orthopedic
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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