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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K130306

INCITE ANCHORED CERVICAL INTERBODY DEVICE · Incite Innovation, LLC · decided 2013-04-11 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-7222INCITE INNOVATIONOVEB0382272221
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-7225INCITE INNOVATIONOVEB038227225
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-7221INCITE INNOVATIONOVEB0382272211
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-7225INCITE INNOVATIONOVEB0382272251
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-7220INCITE INNOVATIONOVEB0382272201
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-7222INCITE INNOVATIONOVEB038227222
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-7221INCITE INNOVATIONOVEB038227221
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-7224INCITE INNOVATIONOVEB038227224
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-7224INCITE INNOVATIONOVEB0382272241
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-7223INCITE INNOVATIONOVEB0382272231
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-7223INCITE INNOVATIONOVEB038227223
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-7220INCITE INNOVATIONOVEB038227220