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Solitaire™ X-PACK

FDA UDI

Class II (US FDA UDI)

by Micro Therapeutics, Inc.

Identity

Trade Name
Solitaire™ X-PACK FDA UDI
Generic Name
Thrombectomy wire-net FDA UDI
Device Name
KIT XPACK201 V01 US FDA UDI
Model / Reference
XPACK201 FDA UDI
Description
KIT XPACK201 V01 US FDA UDI

Identifiers

Primary DI / UDI-DI
00763000270179 FDA UDI
510(k) Number
K091559 FDA UDI
K183022 FDA UDI
FDA Product Code
POL FDA UDI
KRA FDA UDI
NRY FDA UDI
GMDN Term
Thrombectomy wire-net FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5600 FDA UDI
870.1210 FDA UDI
870.1250 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

Yes

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-PACK 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 73f15930-e3bd-419f-bd70-5c1e92fbf980 35 fields · synced Jun 8, 2026