FDA.reportPublic FDA data

PIPELINE

Primary DI
00847536009585
Brand
PIPELINE
Company
Micro Therapeutics, Inc.
Model
FA-71450-30
Device description
FA-71450-30 PIPELINE EMB DEVICE
Published
2015-04-03
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Conditional
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
OUTIntracranial aneurysm flow diverter

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
OUTIntracranial Aneurysm Flow DiverterUnknown3

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
P100018004

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
P100018004PIPELINE EMBOLIZATION DEVICEMicro Therapeutics, Inc. d/b/a ev3 Neurovascular2011-04-06OUT

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00847536009585PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00847536009585008475360095858475360095850847536009585

GMDN Terms#

Term, Definition table
TermDefinition
Bare-metal intracranial vascular stentA sterile non-bioabsorbable tubular device typically intended to be implanted into the base or parent artery of an intracranial aneurysm (e.g., wide-neck aneurysm situated at the base of a bifurcation) to facilitate the delivery of embolics to fill the aneurysm, facilitate clotting within the aneurysm by slowing blood flow into it, and/or to provide support for a neurovascular embolization coil placed inside the aneurysm. It is made of uncoated metal [e.g., nickel-titanium alloy (Nitinol)] and self-expands after it is delivered to the site of implantation and released (e.g., from a dedicated delivery instrument). Disposable devices associated with implantation may be included.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)633-8766Corporate.UDI@medtronic.com

Regulatory Flags#

DUNS number
826110710
Device count
1
Lot or batch
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00763000974077Riptide™MAT-110-1102026-03-30
00763000290702Instant DetacherID-1-52023-01-30
00763000950750Riptide™ Aspiration PumpMAP-10002026-03-09
00763000491772Avyon™ 8FR Balloon Guide Catheter8F-087-85CM2021-04-15
00763000491789Avyon™ 8FR Balloon Guide Catheter8F-087-95CM2021-04-15
00763000915681Riptide™ Aspiration PumpLMT-RAP2025-08-18
00763000925338OnyxTM Liquid Embolic System (LES)105-7100-0602026-01-02
00763000925352OnyxTM Liquid Embolic System (LES)105-7100-0802026-01-02
00847536026834RebarTM105-5081-1532017-04-14
00763000974091Riptide™MAC-12002025-12-13
00763000294236HyperForm104-44202020-08-01
00763000294298HyperForm104-47152020-08-01
00836462002180RebarTM105-5081-1302015-10-09
00847536005471HyperFormTM104-44202016-08-19
00847536005549HyperFormTM104-44702016-04-05
00847536005792HyperFormTM104-47152016-08-14
00836462002197Rebar105-5081-1532015-10-22
00763000294267HyperForm104-44702020-08-01
00763000294328HyperForm104-47702020-08-01
00836462002135Rebar105-5080-1532015-10-09

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00842429106570StentMicrovention, Inc.OUT2025-04-22
00842429106587StentMicrovention, Inc.OUT2025-04-22
00842429106594StentMicrovention, Inc.OUT2025-04-22
00842429106600StentMicrovention, Inc.OUT2025-04-22
00842429106617StentMicrovention, Inc.OUT2025-04-22
00842429106624StentMicrovention, Inc.OUT2025-04-22
00842429106631StentMicrovention, Inc.OUT2025-04-22
00842429106648StentMicrovention, Inc.OUT2025-04-22
00842429106655StentMicrovention, Inc.OUT2025-04-22
00842429106662StentMicrovention, Inc.OUT2025-04-22
00842429106679StentMicrovention, Inc.OUT2025-04-22
00842429106686StentMicrovention, Inc.OUT2025-04-22
00842429106693StentMicrovention, Inc.OUT2025-04-22
00842429106709StentMicrovention, Inc.OUT2025-04-22
00842429106723StentMicrovention, Inc.OUT2025-04-22
00842429106730StentMicrovention, Inc.OUT2025-04-22
00842429106747StentMicrovention, Inc.OUT2025-04-22
00842429106754StentMicrovention, Inc.OUT2025-04-22
00842429106761StentMicrovention, Inc.OUT2025-04-22
00842429106778StentMicrovention, Inc.OUT2025-04-22
00842429106785StentMicrovention, Inc.OUT2025-04-22
00842429106792StentMicrovention, Inc.OUT2025-04-22
00842429106808StentMicrovention, Inc.OUT2025-04-22
00842429106815StentMicrovention, Inc.OUT2025-04-22
00842429106822StentMicrovention, Inc.OUT2025-04-22
00842429106839StentMicrovention, Inc.OUT2025-04-22
00842429106846StentMicrovention, Inc.OUT2025-04-22
00842429106853StentMicrovention, Inc.OUT2025-04-22
00842429106860StentMicrovention, Inc.OUT2025-04-22
00763000448929Pipeline TM Flex Embolization Device with Shield Technology TMMicro Therapeutics, Inc.OUT2025-03-11