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

Clearance record K122008

INCITE ANCHORED CERVICAL INTERBODY (ACI) FUSION DEVICE · Incite Innovation, LLC · decided 2012-11-16 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-9212-LONGINCITE INNOVATIONOVEB038229212LONG1
INCITE INNOVATION ANCHORED CERVICAL INERBODY DEVICE22-9223INCITE INNOVATIONOVEB0382292231
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-9224INCITE INNOVATIONOVEB0382292241
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-9221INCITE INNOVATIONOVEB038229221
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-9224INCITE INNOVATIONOVEB038229224
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-9222INCITE INNOVATIONOVEB0382292221
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-9222INCITE INNOVATIONOVEB038229222
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-9221INCITE INNOVATIONOVEB0382292211
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-9211-SHORTINCITE INNOVATIONOVEB038229211SHORT1
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-9220INCITE INNOVATIONOVEB038229220
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-9225INCITE INNOVATIONOVEB0382292251
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-9225INCITE INNOVATIONOVEB038229225
INCITE INNOVATION ANCHORED CERVICAL INTERBODY DEVICE22-9220INCITE INNOVATIONOVEB0382292201
INCITE INNOVATION ANCHORED CERVICAL INERBODY DEVICE22-9223INCITE INNOVATIONOVEB038229223