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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: NUVASIVE, INC. COROENT INTERLOCK SYSTEM; INTERVERTEBRAL FUSION DEVICE WITH INTEGRATED FIXATION, CERVICAL
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NUVASIVE, INC. COROENT INTERLOCK SYSTEM; INTERVERTEBRAL FUSION DEVICE WITH INTEGRATED FIXATION, CERVICAL Back to Search Results
Model Number 6790226
Medical Device Problem Code Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code Swelling (2091)
Date of Event 10/07/2015
Type of Reportable Event Serious Injury
Additional Manufacturer Narrative
No allegation of product malfunction has been reported, no x-rays were provided to confirm the alleged event.Product remains in-situ.Product remains in-situ.
 
Event or Problem Description
On (b)(6) 2015 patient underwent an anterior cervical discectomy and fusion procedure.As per reporter approximately 5 days postoperatively, the patient was found to have collection of serosanguinous fluid with swelling.The sutures were opened, wound was suctioned out and irrigated with antibiotic solution.Wound was closed with no reported complications.
 
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Brand Name
COROENT INTERLOCK SYSTEM
Common Device Name
INTERVERTEBRAL FUSION DEVICE WITH INTEGRATED FIXATION, CERVICAL
Manufacturer (Section D)
NUVASIVE, INC.
7475 lusk blvd
san diego CA 92121
MDR Report Key7601593
Report Number2031966-2018-00104
Device Sequence Number13505344
Product Code OVE
UDI-Device Identifier00887517361615
UDI-Public00887517361615
Combination Product (Y/N)N
Initial Reporter StateCA
Initial Reporter CountryUS
PMA/510(K) Number
K102547
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2015
Reporter Type Manufacturer
Report Source company representative,health
Initial Reporter Occupation Physician
Type of Report Initial
Report Date (Section B) 06/14/2018
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Operator of Device Physician
Device Model Number6790226
Was Device Available for Evaluation? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 05/17/2018
Initial Report FDA Received Date06/14/2018
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)		 No
Patient Sequence Number1
Outcome Attributed to Adverse Event Hospitalization;
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