HOTWIRE™ RF GUIDEWIRE

Primary DI
00850057445244
Brand
HOTWIRE™ RF GUIDEWIRE
Company
Atraverse Medical, Inc
Model
901024
Catalog number
H1P-035-230-LAA-0
Device description
The HOTWIRE™ is a sterile, single-use guidewire device that delivers radiofrequency (RF) power in a monopolar mode to a distal electrode segment for the creation of an atrial septal defect in the heart. The HOTWIRE™ is intended to be used in conjunction with compatible previously cleared intravascular sheaths and/or dilators, and previously cleared RF electrosurgical generator(s).The HOTWIRE™ is comprised of a stainless steel core wire. The main body of the wire is jacketed with an insulating polymer that provides electrical insulation and facilitates smooth movement of the device through vascular dilators and/or sheaths. The floppy distal segment of the wire has an atraumatic tip with an uninsulated stainless-steel coil, which serves as an electrode, and also provides fluoroscopic and/or echogenic visualization. A tungsten marker coil at the tip provides additional radiopacity. The stiff body of the HOTWIRE™ provides support for advancing wire-guided devices into the left atrium after the distal segment has traversed the septum. The proximal insulated portion of the wire has visual markers that align the electrode tip with 3rd party transseptal sheaths and/or dilators. A portion of the proximal wire is uninsulated for placement of an included Adapter Pin that connects to hand pieces used with compatible previously cleared RF electrosurgical generators.
Published
2025-06-12
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
DXFCatheter, Septostomy

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DXFCatheter, SeptostomyCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K240900000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K240900000HOTWIRE™ RF GuidewireAtraverse Medical2024-05-01DXF

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00850057445244PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00850057445244008500574452448500574452440850057445244

GMDN Terms#

Term, Definition table
TermDefinition
Cardiac transseptal access setA collection of nonimplantable, invasive devices intended to be used to puncture the interatrial septum during a transseptal catheterization procedure, and to create a conduit for the introduction of various cardiovascular catheters into the left side of the heart. It includes a vascular guide-catheter (which may be referred to as a steerable introducer) with a transseptal needle to create the puncture, and typically includes additional introduction assistive devices necessary for the procedure (e.g., stylet, guidewire, dilator). This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Guidewire Diameter0.035Inch
Guidewire Length230Centimeter

Sterilization Methods#

Method table
Method
Radiation Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1 760-278-8098info@atraversemedical.com

Regulatory Flags#

DUNS number
118954537
Device count
1
Lot or batch
true
Expiration date on label
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00850057445275HOTWIRE™ RF GUIDEWIRE902002H2J-032-180-ABT-02025-10-01
00850057445282HOTWIRE™ RF GUIDEWIRE902003H2P-032-180-ABT-02025-10-01
00850057445299HOTWIRE™ RF GUIDEWIRE902004H2S-032-230-ABT-02025-10-01
00850057445305HOTWIRE™ RF GUIDEWIRE902005H2J-032-230-ABT-02025-10-01
00850057445312HOTWIRE™ RF GUIDEWIRE902006H2P-032-230-ABT-02025-10-01
00850057445329HOTWIRE™ RF GUIDEWIRE902007H2S-032-180-BWI-02025-10-01
00850057445336HOTWIRE™ RF GUIDEWIRE902008H2J-032-180-BWI-02025-10-01
00850057445343HOTWIRE™ RF GUIDEWIRE902009H2P-032-180-BWI-02025-10-01
00850057445350HOTWIRE™ RF GUIDEWIRE902010H2S-032-230-BWI-02025-10-01
00850057445367HOTWIRE™ RF GUIDEWIRE902011H2J-032-230-BWI-02025-10-01
00850057445374HOTWIRE™ RF GUIDEWIRE902012H2P-032-230-BWI-02025-10-01
00850057445381HOTWIRE™ RF GUIDEWIRE902013H2S-035-180-MDT-02025-10-01
00850057445398HOTWIRE™ RF GUIDEWIRE902014H2J-035-180-MDT-02025-10-01
00850057445404HOTWIRE™ RF GUIDEWIRE902015H2P-035-180-MDT-02025-10-02
00850057445411HOTWIRE™ RF GUIDEWIRE902016H2S-035-230-MDT-02025-10-02
00850057445428HOTWIRE™ RF GUIDEWIRE902017H2J-035-230-MDT-02025-10-02
00850057445435HOTWIRE™ RF GUIDEWIRE902018H2P-035-230-MDT-02025-10-02
00850057445442HOTWIRE™ RF GUIDEWIRE902019H2S-035-180-LAA-02025-10-02
00850057445459HOTWIRE™ RF GUIDEWIRE902020H2J-035-180-LAA-02025-10-02
00850057445466HOTWIRE™ RF GUIDEWIRE902021H2P-035-180-LAA-02025-10-02

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00858769006487SafeSept RF Transseptal GuidewirePPMDMDXF2026-03-23
00858769006500SafeSept RF Transseptal GuidewirePPMDMDXF2026-03-23
00858769006524SafeSept RF Transseptal GuidewirePPMDMDXF2026-03-23
00858769006531SafeSept RF Transseptal GuidewirePPMDMDXF2026-03-23
00858769006548SafeSept RF Transseptal GuidewirePPMDMDXF2026-03-23
00858769006555SafeSept RF Transseptal GuidewirePPMDMDXF2026-03-23
30858769006488SafeSept RF Transseptal GuidewirePPMDMDXF2026-03-23
00858769006494SafeSept RF Transseptal GuidewirePPMDMDXF2026-03-23
30858769006501SafeSept RF Transseptal GuidewirePPMDMDXF2026-03-23
00858769006517SafeSept RF Transseptal GuidewirePPMDMDXF2026-03-23
30858769006525SafeSept RF Transseptal GuidewirePPMDMDXF2026-03-23
30858769006532SafeSept RF Transseptal GuidewirePPMDMDXF2026-03-23
30858769006549SafeSept RF Transseptal GuidewirePPMDMDXF2026-03-23
30858769006556SafeSept RF Transseptal GuidewirePPMDMDXF2026-03-23
00850057445404HOTWIRE™ RF GUIDEWIREAtraverse Medical, IncDXF2025-10-02
00850057445411HOTWIRE™ RF GUIDEWIREAtraverse Medical, IncDXF2025-10-02
00850057445428HOTWIRE™ RF GUIDEWIREAtraverse Medical, IncDXF2025-10-02
00850057445435HOTWIRE™ RF GUIDEWIREAtraverse Medical, IncDXF2025-10-02
00850057445442HOTWIRE™ RF GUIDEWIREAtraverse Medical, IncDXF2025-10-02
00850057445459HOTWIRE™ RF GUIDEWIREAtraverse Medical, IncDXF2025-10-02
00850057445466HOTWIRE™ RF GUIDEWIREAtraverse Medical, IncDXF2025-10-02
00850057445473HOTWIRE™ RF GUIDEWIREAtraverse Medical, IncDXF2025-10-02
00850057445480HOTWIRE™ RF GUIDEWIREAtraverse Medical, IncDXF2025-10-02
00850057445497HOTWIRE™ RF GUIDEWIREAtraverse Medical, IncDXF2025-10-02
00850057445503HOTWIRE™ RF GUIDEWIREAtraverse Medical, IncDXF2025-10-02
00850057445510HOTWIRE™ RF GUIDEWIREAtraverse Medical, IncDXF2025-10-02
00850057445275HOTWIRE™ RF GUIDEWIREAtraverse Medical, IncDXF2025-10-01
00850057445282HOTWIRE™ RF GUIDEWIREAtraverse Medical, IncDXF2025-10-01
00850057445299HOTWIRE™ RF GUIDEWIREAtraverse Medical, IncDXF2025-10-01
00850057445305HOTWIRE™ RF GUIDEWIREAtraverse Medical, IncDXF2025-10-01