K242419 is an FDA 510(k) clearance for the 018 Hydrophilic Coated OTW PTA Balloon Dilatation Catheter. This device is classified as a Catheter, Angioplasty, Peripheral, Transluminal (Class II - Special Controls, product code LIT).
Submitted by Creagh Medical Ltd. Dba Surmodics, Inc. (Ballinasloe, IE). The FDA issued a Cleared decision on November 15, 2024, 92 days after receiving the submission on August 15, 2024.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1250.
| 510(k) Number | K242419 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 15, 2024 |
| Decision Date | November 15, 2024 |
| Days to Decision | 92 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | LIT - Catheter, Angioplasty, Peripheral, Transluminal |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1250 |