Pounce ™ Thrombectomy
GUDID 00812339030326
Pounce Arterial Thrombectomy System with Handle
Surmodics, Inc.
Thrombectomy suction catheter| Primary Device ID | 00812339030326 |
| NIH Device Record Key | 85ec1d94-f784-4e59-8f6c-8619f6c1403a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pounce ™ Thrombectomy |
| 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
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
| Guidewire Compatibility | 7 French |
| Catheter Length | 135 Centimeter |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00812339030326 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K220501
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 | 2024-10-28 |
| Device Publish Date | 2024-10-18 |
On-Brand Devices [Pounce ™ Thrombectomy]
| 00812339030784 | Pounce Arterial Packaged Assembly, Sterile |
| 00812339030326 | Pounce Arterial Thrombectomy System with Handle |
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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