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Solitaire™ X

FDA UDI

Class II (US FDA UDI)

by Micro Therapeutics, Inc.

Identity

Trade Name
Solitaire™ X FDA UDI
Generic Name
Thrombectomy wire-net FDA UDI
Device Name
STENT SFR4-6-24-06 V03 SOLITIARE4 FDA UDI
Model / Reference
SFR4-6-24-06 FDA UDI
Description
STENT SFR4-6-24-06 V03 SOLITIARE4 FDA UDI

Identifiers

Primary DI / UDI-DI
00763000425715 FDA UDI
510(k) Number
K183022 FDA UDI
K193576 FDA UDI
FDA Product Code
NRY FDA UDI
POL FDA UDI
GMDN Term
Thrombectomy wire-net FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1250 FDA UDI
882.5600 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Thrombectomy wire-net

Solitaire™ X by Micro Therapeutics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thrombectomy wire-net.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 26db72b6-e9d5-4177-b84a-ebeba2b4f471 36 fields · synced May 30, 2026