ARTHROSCOPE 275-756-000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1996-02-14 for ARTHROSCOPE 275-756-000 manufactured by Stryker Endoscopy Div. Stryker Corp..

Event Text Entries

[17376] Possible product problem; during arthroscopy, a small piece of metal was seen. Rptr questions if it breaks off from knee shaver. 3 possible boxes with 3 (packaging not saved). 1. 95096352, 2. 96015012, 3. 93126682.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW1008332
MDR Report Key30211
Date Received1996-02-14
Date of Report1996-02-11
Date of Event1996-01-22
Date Added to Maude1996-02-20
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA0
Report to FDA0
Event Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameARTHROSCOPE
Generic NameARTHROSCOPE
Product CodeLLO
Date Received1996-02-14
Catalog Number275-756-000
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Implant FlagN
Date RemovedB
Device Sequence No1
Device Event Key30933
ManufacturerSTRYKER ENDOSCOPY DIV. STRYKER CORP.
Manufacturer AddressSAN JOSE CA 95134 US


Patients

Patient NumberTreatmentOutcomeDate
10 1996-02-14

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