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CORUS™ Allograft Delivery Instrument

FDA UDI

Class I (US FDA UDI)

by Providence Medical Technology, Inc.

Identity

Trade Name
CORUS™ Allograft Delivery Instrument FDA UDI
Generic Name
Orthopaedic graft guide FDA UDI
Device Name
A manual orthopedic surgical instrument used to deliver structural bone graft to a target area of the spine. The Allograft Delivery Instrument is manufactured using medical grade polycarbonate resin and stainless steel. The CORUS™ Allograft Delivery Instrument is intended and indicated for the delivery of structural bone graft to a target area of the spine. FDA UDI
Model / Reference
PD-10-400 FDA UDI
Description
A manual orthopedic surgical instrument used to deliver structural bone graft to a target area of the spine. The Allograft Delivery Instrument is manufactured using medical grade polycarbonate resin and stainless steel. The CORUS™ Allograft Delivery Instrument is intended and indicated for the delivery of structural bone graft to a target area of the spine. FDA UDI

Identifiers

Primary DI / UDI-DI
00852776006454 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic graft guide FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic graft guide

CORUS™ Allograft Delivery Instrument by Providence Medical Technology, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic graft guide.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0c57669b-d50b-40af-a21f-c29fabb991d5 34 fields · synced Jun 8, 2026