Pounce™ Thrombectomy System
GUDID 00812339030296
The Surmodics™ Pounce™ Thrombus Retrieval System is a percutaneous catheter system designed to facilitate mechanical thrombus removal in the arterial peripheral vasculature.
Surmodics, Inc.
Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter| Primary Device ID | 00812339030296 |
| NIH Device Record Key | 5af58768-490d-4207-93e0-2b3ab5331f2c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pounce™ Thrombectomy System |
| Version Model Number | PTS-0607-7F135 |
| Company DUNS | 098414659 |
| Company Name | Surmodics, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Device Dimensions
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00812339030296 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K192814
FDA Product Code
| QEW | Peripheral Mechanical Thrombectomy With Aspiration |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-01-04 |
| Device Publish Date | 2021-12-27 |
Devices Manufactured by Surmodics, Inc.
| 00812339030791 - Pounce™ Venous Thrombectomy System | 2024-06-17 Pounce Venous Thrombectomy System |
| 00812339030760 - Pounce ™ LP Thrombectomy | 2024-03-27 Pounce LP Thrombectomy System |
| 00812339030319 - Pounce Venous Thrombectomy System | 2023-11-06 Pounce Venous Thrombectomy System |
| 00812339030333 - SurVeil DCB | 2023-10-12 SurVeil DCB 4.0mm x 40mm x 135cm |
| 00812339030340 - SurVeil DCB | 2023-10-12 SurVeil DCB 4.0mm x 60mm x 135cm |
| 00812339030357 - SurVeil DCB | 2023-10-12 SurVeil DCB 4.0mm x 80mm x 135cm |
| 00812339030364 - SurVeil DCB | 2023-10-12 SurVeil DCB 4.0mm x 100mm x 135cm |
| 00812339030371 - SurVeil DCB | 2023-10-12 SurVeil DCB 4.0mm x 120mm x 135cm |
Trademark Results [Pounce]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 POUNCE 98577012 not registered Live/Pending |
Kureha America, Inc. 2024-05-30 |
 POUNCE 88983661 not registered Live/Pending |
MIG Global LLC 2019-06-10 |
 POUNCE 88979781 not registered Live/Pending |
MIG Global LLC 2019-06-10 |
 POUNCE 88466864 not registered Live/Pending |
MIG Global LLC 2019-06-10 |
 POUNCE 88396514 not registered Live/Pending |
Surmodics, Inc. 2019-04-22 |
 POUNCE 88107569 not registered Live/Pending |
PounceLaw LLC 2018-09-06 |
 POUNCE 87196680 not registered Dead/Abandoned |
Gilbert, Michael 2016-10-07 |
 POUNCE 86712021 not registered Dead/Abandoned |
SERVIUS, GARY S 2015-07-31 |
 POUNCE 86352010 5013450 Live/Registered |
P&N TECHNOLOGIES, LLC 2014-07-30 |
 POUNCE 86211549 not registered Dead/Abandoned |
Mint Digital Ltd. 2014-03-05 |
 POUNCE 85520427 4299196 Live/Registered |
Cortland Research, LLC 2012-01-19 |
 POUNCE 77802734 not registered Dead/Abandoned |
Del Monte Corporation 2009-08-12 |
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