BONE ELEVATOR 17MM WI.240MM FK171R

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-12-16 for BONE ELEVATOR 17MM WI.240MM FK171R manufactured by Aesculap Ag.

Event Text Entries

[62960893] (b)(4). Manufacturing site evaluation: evaluation on-going.
Patient Sequence No: 1, Text Type: N, H10


[62960894] Country of complaint: (b)(6). During a knee surgery the bone elevator device broke.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2916714-2016-01054
MDR Report Key6181913
Date Received2016-12-16
Date of Report2017-09-20
Date of Event2016-11-18
Date Facility Aware2016-12-09
Date Mfgr Received2016-11-24
Device Manufacturer Date2016-08-16
Date Added to Maude2016-12-16
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. NICOLE BROYLES
Manufacturer Street615 LAMBERT POINTE DRIVE
Manufacturer CityHAZELWOOD MO 63042
Manufacturer CountryUS
Manufacturer Postal63042
Manufacturer Phone3145515988
Manufacturer G1AESCULAP AG
Manufacturer StreetPO BOX 40
Manufacturer CityTUTTLINGEN, 78501
Manufacturer CountryGM
Manufacturer Postal Code78501
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameBONE ELEVATOR 17MM WI.240MM
Generic NameGENERAL SURGICAL INSTRUMENTS
Product CodeGEG
Date Received2016-12-16
Returned To Mfg2016-11-30
Model NumberFK171R
Catalog NumberFK171R
Lot Number4507729243
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Age4 MO
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerAESCULAP AG
Manufacturer AddressPO BOX 40 TUTTLINGEN, 78501 GM 78501


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2016-12-16

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