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Vertelink Corporation

3 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
VERTELINK KOBRA SPINAL FIXATION SYSTEM (K032102)Vertelink Corporation2003-12-12
PATHWAY ACCESS SHEATH CATHETER (K030734)Vertelink Corporation2003-09-10
PATHWAY ACCESS SHEATH CATHETER (K030662)Vertelink Corporation2003-09-03

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Every clearance here is in the API, with alerts when new ones post.