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X-STOP® Interspinous Spacer

FDA UDI

Class III (US FDA UDI)

by Medtronic Sofamor Danek, Inc.

Identity

Trade Name
X-STOP® Interspinous Spacer FDA UDI
Generic Name
Lumbar decompression interspinous spacer FDA UDI
Device Name
SPACER 1-2210 US 10MM X STOP FDA UDI
Model / Reference
1-2210 FDA UDI
Description
SPACER 1-2210 US 10MM X STOP FDA UDI

Identifiers

Primary DI / UDI-DI
00858196001895 FDA UDI
PMA Number
P040001 FDA UDI
FDA Product Code
NQO FDA UDI
GMDN Term
Lumbar decompression interspinous spacer FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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
MRI Safety
MR Conditional FDA UDI

Category: Lumbar decompression interspinous spacer

X-STOP® Interspinous Spacer by Medtronic Sofamor Danek, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lumbar decompression interspinous spacer.

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 510935ef-3555-4168-bb55-ea7d2fd301f1 36 fields · synced Jun 8, 2026