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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ALPHATEC SPINE, INC. IDENTITI; INTERVERTEBRAL FUSION DEVICE WITH INTEGRATED FIXATION, LUMBAR

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ALPHATEC SPINE, INC. IDENTITI; INTERVERTEBRAL FUSION DEVICE WITH INTEGRATED FIXATION, LUMBAR Back to Search Results
Model Number 232-11-90-350
Device Problem Fracture (1260)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 09/08/2022
Event Type  malfunction  
Event Description
It was reported during insertion of a graft bolt, the angle was too shallow causing the implant to break.All pieces of the broken implant were removed from the patient.
 
Manufacturer Narrative
The broken implant was discarded at the hospital.No product evaluation possible.The identifying lot number was not provided; therefore, review of the device history records could not be conducted.The root cause is unknown but may be the result of the shallow angle during insertion.If additional information is received, a supplemental report will be submitted.
 
Manufacturer Narrative
This report is being submitted to provide additional information regarding a supplemental investigation conducted by alpahtec for identiti alif intraoperative graft bolt failures.The supplemental investigation was completed on 04-jan-2023.Corrected information: d4: lot# unknown d5: health professional medical device problem code: 1069 additional information: h6: type of investigation: 4102, 3331, 4114 investigation findings: 3243, 4248 investigation conclusion: 19, 61 additional information: the graft bolt is a component of the alphatec identiti alif standalone interbody system, which is an integrated intervertebral body fusion device for use in anterior lumbar interbody fusion (alif) procedures used in patients for treatment, not diagnosis.The broken graft bolt was retrieved from the patient and discarded at the hospital.Photographs/radiographs were not provided to confirm this event.The identifying lot number was not provided.The patient's bone quality and medical history is unknown.No additional information was provided to alpahtec regarding this event.This event was evaluated, and it was determined the alphatec device malfunctioned during insertion.If this event were to reoccur, a portion of the graft bolt potentially could be left in situ which may require subsequent surgical intervention.Based on the information provided, alphatec determined this event is reportable to the fda under 21 cfr 803.Alphatec conducted a supplemental investigation for intraoperative graft bolt failures.The investigation included simulated use activities to replicate failure modes in a controlled setting, both in cadavers and in solid rigid polyurethane foam ("bone foam") and conducted astm testing to benchmark failure torques and understand the potential of failure during reasonable use.Physical characterization and investigation were performed on complaint-related returned materials, where available.Additional testing was performed on material, not distributed, to replicate the failure.The graft bolt is designed to withstand an insertion torque consistent with on-trajectory insertion (40°) into a range of bone qualities representative of the patient population.Mechanical testing performed as a part of the root cause investigation for these reported intraoperative failures demonstrates that the device meets performance specifications required for this device.Both the torque required to fail the graft bolt in torsion and the load required to fail the graft bolt in cantilever bending are greater than those required to fail a more conventional screw common to interfixated lumbar interbody fusion procedures.The following conclusions of the graft bolt intraoperative failure were drawn from the results of the investigation: 1.The failures were not the result of manufacturing defects, as no manufacturing defects were identified in the device history review.2.The failures were not the result of normal use of the graft bolt as prescribed in the surgical technique.The graft bolt was successfully designed to withstand much greater torques than the insertion torque into normal bone; this is reflected in both the stimulated use activities and the various mechanical test conducted.3.The failures were not the result of a performance deficiency in the graft bolt as compared to a more conventional screw design; indeed, the graft bolt is comparable to a conventional screw in insertion torque and outperforms a conventional screw in torsional and bending failure modes.4.The failures were primarily caused by use error.Gross deviation from the prescribed graft bolt insertion trajectory caused the graft bolt to impinge on the posterior end of the medial screw hole or the posterior wall of the interbody spacer.The users then did not react to the increase in insertion torque as they would have with a conventional screw design.With the graft bolt engaged in the porous titanium of the interbody spacer, insertion torque could increase until failure torque for the graft bolt was reached, resulting in shear failure.As a result of the supplemental investigation, alphatec has implemented labeling changes in the surgical technique guide and the instructions for use, prescribing the use of hole preparation instruments, cautioning against off-trajectory insertion, and warning of potential device failure in off-trajectory insertion conditions.On (b)(6), 2023, a field bulletin was sent alphatec sales force and customer service notifying them of the changes.Labeling review: "warnings/cautions/precautions: care should be taken in performing screw hole preparation to facilitate a proper graft bolt insertion trajectory and implantation.Confirm under fluoroscopy that the graft bolt insertion angle is as close as possible to a 40° trajectory.A shallow or incorrect graft bolt trajectory may result in encroachment of the spacer and lead to graft bolt breakage." on (b)(6) 2022, the fda sent alphatec additional information request for this mdr.Alphatec responded to the fda on (b)(6) 2023.
 
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Brand Name
IDENTITI
Type of Device
INTERVERTEBRAL FUSION DEVICE WITH INTEGRATED FIXATION, LUMBAR
Manufacturer (Section D)
ALPHATEC SPINE, INC.
1950 camino vida roble
carlsbad CA 92008
Manufacturer Contact
wesley channell
1950 camino vida roble
carlsbad, CA 92008
9014283693
MDR Report Key15564205
MDR Text Key304612340
Report Number2027467-2022-00065
Device Sequence Number1
Product Code OVD
UDI-Device Identifier00190376370330
UDI-Public00190376370330
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K203742
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Health Professional
Reporter Occupation Non-Healthcare Professional
Type of Report Initial,Followup
Report Date 09/08/2022
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Model Number232-11-90-350
Device Catalogue Number232-11-90-350
Was Device Available for Evaluation? No
Initial Date Manufacturer Received 09/08/2022
Initial Date FDA Received10/07/2022
Supplement Dates Manufacturer Received09/08/2022
Supplement Dates FDA Received01/24/2023
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
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