MAUDE Adverse Event Report: OXFORD PERFORMANCE MATERIALS, INC. HTR-PEKK; CRANIAL IMPLANT

Model Number	PK618173
Health Effect - Clinical Code	Post Operative Wound Infection (2446)
Date of Event	01/04/2017
Event or Problem Description
The implant was removed due to an infection.The cause or the source of the infection are unknown.The implant is shipped non-sterile and then sterilized at the healthcare facility according to the instructions for use.There are no sterilization, pathology, or surgical records available.

• Brand Name: HTR-PEKK
• Common Device Name: CRANIAL IMPLANT
• Manufacturer (Section D): OXFORD PERFORMANCE MATERIALS, INC.; p.o. box 585; 30 south satellite road; south windsor CT 06074
• MDR Report Key: 6264482
• Report Number: 3009582362-2017-00001
• Device Sequence Number: 13465287
• Product Code: GXN
• UDI-Device Identifier: 00813298023831
• UDI-Public: 00813298023831
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: K121818
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2016
• Device Explanted Year: 2017
• Reporter Type: Manufacturer
• Report Source: distributor
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 01/19/2017

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?: No
• Operator of Device: No Information
• Device Model Number: PK618173
• Device Lot Number: IG5775M-11F001
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/06/2017
• Initial Report FDA Received Date: 01/19/2017
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 50 YR