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CORNERSTONE® PSR Cervical Fusion System

FDA UDI

Class II (US FDA UDI)

by Medtronic Sofamor Danek, Inc.

Identity

Trade Name
CORNERSTONE® PSR Cervical Fusion System FDA UDI
Generic Name
Orthopaedic graft inserter, reusable FDA UDI
Device Name
INSERTER X1111080 CERVICAL THRDED W STOP FDA UDI
Model / Reference
X1111080 FDA UDI
Description
INSERTER X1111080 CERVICAL THRDED W STOP FDA UDI

Identifiers

Primary DI / UDI-DI
00643169122673 FDA UDI
510(k) Number
K111264 FDA UDI
FDA Product Code
ODP FDA UDI
GMDN Term
Orthopaedic graft inserter, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic graft inserter, reusable

CORNERSTONE® PSR Cervical Fusion System by Medtronic Sofamor Danek, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic graft inserter, reusable.

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 3319239a-2373-4747-887d-c536261b3c4b 35 fields · synced May 30, 2026