MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS, INC. ATTUNE NOTCH GUIDE SZ 8; KNEE INSTRUMENT/TRIAL

Model Number	2545-00-028
Medical Device Problem Codes	Bent (1059); Material Erosion (1214)
Health Effect - Clinical Code	No Information (3190)
Date of Event	05/24/2017
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.This complaint is still under investigation.Depuy will notify the fda of the results of this investigation once it has been completed.
Event or Problem Description
It was reported that upon checking the instrument pan post surgery, it was discovered that the middle part of notch guide was bent and scratched/scored.
Additional Manufacturer Narrative
Examination of the returned device confirmed the reported event of damage.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.

• Brand Name: ATTUNE NOTCH GUIDE SZ 8
• Common Device Name: KNEE INSTRUMENT/TRIAL
• Manufacturer (Section D): DEPUY ORTHOPAEDICS, INC.; 700 orthopaedic drive; warsaw IN 46582
• MDR Report Key: 6659743
• Report Number: 1818910-2017-19928
• Device Sequence Number: 2065021
• Product Code: JWH
• UDI-Device Identifier: 10603295130451
• UDI-Public: (01)10603295130451
• Combination Product (Y/N): N
• Initial Reporter State: NC
• Initial Reporter Country: US
• PMA/510(K) Number: K140881
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: distributor
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 05/24/2017

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
• Operator of Device: Health Professional
• Device Model Number: 2545-00-028
• Device Catalogue Number: 254500028
• Device Lot Number: PG239021
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 06/03/2017
• Initial Date Received by Manufacturer: 05/24/2017
• Supplement Date Received by Manufacturer: 07/20/2017
• Initial Report FDA Received Date: 06/22/2017
• Supplement Report FDA Received Date: 07/23/2017
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1