MAUDE Adverse Event Report: SPECTRANETICS ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW); CATHETER, PERCUTANEOUS, CUTTING/SCORING

Model Number	2092-4040
Medical Device Problem Code	Material Rupture (1546)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	12/09/2020
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The patent's dob or age at time of event, gender, weight, ethnicity, and race are unknown.This information was not available from the facility.During inflation, the balloon ruptured at rbp.No patient injury, this mdr is being reported conservatively.Foreign- (b)(6).The angiosculpt device was discarded by the facility , thus no returned product investigation was performed.
Event or Problem Description
The angiosculpt device was used to treat a moderately calcified and severely tortuous sfa.During the first inflation at 14 atm for 1 minute, the balloon ruptured.The procedure was completed with a competitor device.No patient injury reported.
Event or Problem Description
The angiosculpt device was used to treat a moderately calcified sfa.During the first inflation at 14 atm for 1 minute, the balloon ruptured.The procedure was completed with a competitor device.No patient injury reported.
Additional Manufacturer Narrative
Block b5: the vessel tortuosity is unknown; therefore, it was removed from the complaint details.

• Brand Name: ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)
• Common Device Name: CATHETER, PERCUTANEOUS, CUTTING/SCORING
• Manufacturer (Section D): SPECTRANETICS; 5055 brandin court; fremont CA 94538
• MDR Report Key: 11032898
• Report Number: 3005462046-2020-00056
• Device Sequence Number: 2692238
• Product Code: PNO
• UDI-Device Identifier: 00813132021405
• UDI-Public: 00813132021405
• Combination Product (Y/N): Y
• Initial Reporter Country: JA
• PMA/510(K) Number: K100303
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 12/10/2020

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 Expiration Date: 01/10/2023
• Device Model Number: 2092-4040
• Device Catalogue Number: 2092-4040
• Device Lot Number: G20010011
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: Not provided
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 12/17/2020
• Supplement Report FDA Received Date: 12/18/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: CORDIS: 0.018" CHEVALIER FLOPPY GUIDE WIRE; MEDIKIT: PARENT PLUS 45 SHEATH/GUIDE SIZE UNK
• Outcome Attributed to Adverse Event: Other