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ZIP LP (REF 103-010-035)Recalls & reported problems

Aurora Spine, Inc. · ZIP LP MIS Interspinous Fusion System, 10mm X 35mm · Class 2

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 B5211030100350), received between Jun 26, 2021 and Jun 26, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Detachment of Device or Device Component1

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 26, 2021Detachment of Device or Device Component; Detachment of Device or Device Component

    ON 27 MAY 2021, A SALES REPRESENTATIVE RELAYED INFORMATION FROM A DOCTOR THAT TWO ZIP DEVICES PARTIALLY OPENED FOLLOWING A LUMBAR FUSION. THE PARTIAL OPENING IS VISIBLE ON XRAY. NO PATIENT PROBLEMS REPORTED. NO EXPLANT PERFORMED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12072876 ↗

Other Spinous Process Plate devices

All Spinous Process Plate devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.