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SurfRider 13 Microcatheter
KANEKA AMERICAS HOLDING INC · Model N01-13165-PS · UDI-DI 00810201980014
1
510(k) clearances
1,766
Adverse events (49 deaths)
7
Recalls
75
Facilities
Description
SurfRider 13 Microcatheters are single lumen devices designed to aid the physician in accessing distal neuro vasculature when used with a guide catheter and steerable guidewire. There are two models of the SurfRider 13 Microcatheter, steam shapeable straight tip and a pre-shaped J tip. Both have an effective length of 165cm. The microcatheter is packaged and sterilized with the shaping mandrel and an intruder sheath. This model is the pre-shaped tip.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-01-16 | Scientia Vascular, Inc. | Due to manufacturing non-conformance that resulted in channels in the seal on the packaging pouch. As a result, this could potential create a breach in the sterile barrier. |
| 2024-08-30 | Stryker Neurovascular | Stryker Neurovascular has observed that devices with Out of United States (OUS) approved Instructions for Use (IFU) and Packaging Labels (pouch and carton), different configuration |
| 2024-04-23 | Stryker Neurovascular | Neurovascular devices did not meet the minimum sample size required for endotoxin testing during manufacturing processes and are out of compliance with the AAMI ST72 standard, so t |
| 2024-03-08 | ROUTE 92 MEDICAL INC | Their is the potential for distal tip separation at the proximal marker band of the delivery catheters. |
| 2024-03-08 | ROUTE 92 MEDICAL INC | Their is the potential for distal tip separation at the proximal marker band of the delivery catheters |
| 2024-02-02 | Medos International Sarl | Medos has received an increase in complaints for CEREBASE DA Guide Sheath with reports of fractures at the distal end, which may result in surgical procedural delay, vascular injur |
| 2023-12-06 | Stryker, Inc. | The microcatheter IFU contains an intended use that has not been evaluated by the FDA. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.