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CoRoent 6770815CP2Recalls & reported problems

Nuvasive, Inc. · Interlock II Ti-C, 8x17x14mm 15° · Class 2 · Implant

All models of CoRoent (64)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887517812452), received between Jun 15, 2022 and Jun 15, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fracture” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Fracture1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJun 15, 2022Fracture; Fracture

    ON (B)(6) 2022 A PATIENT UNDERWENT AN ANTERIOR CERVICAL INTERBODY FUSION PROCEDURE ON UNKNOWN LEVELS OF THE SPINE. DURING THE PROCEDURE DURING IMPLANT INSERTION THE CAGE CRACKED DOWN THE MIDDLE. IT IS UNKNOWN WHETHER THE CRACKED DEVICE REMAINED IN-SITU OR WAS REMOVED FROM THE PATIENT. NO INJURY OR ADVERSE EFFECTS TO THE PATIENT WERE REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14691770 ↗

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Sources and updates

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