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CORUS PCSS Implant 4mm

FDA UDI

by Providence Medical Technology, Inc.

Identity

Trade Name
CORUS PCSS Implant 4mm FDA UDI
Generic Name
Implantable cervical facet joint distractor FDA UDI
Device Name
CORUS™ PCSS is posterior spinal instrumentation with integrated screw fixation intended to provide immobilization and stabilization of spinal segments. FDA UDI
Model / Reference
DX-50-403 FDA UDI
Description
CORUS™ PCSS is posterior spinal instrumentation with integrated screw fixation intended to provide immobilization and stabilization of spinal segments. FDA UDI

Identifiers

Primary DI / UDI-DI
00852776006645 FDA UDI
GMDN Term
Implantable cervical facet joint distractor FDA UDI

Classification

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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Implantable cervical facet joint distractor

CORUS PCSS Implant 4mm by Providence Medical Technology, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable cervical facet joint distractor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c20e91bc-1008-498d-ba06-3b0e6e953b0d 33 fields · synced May 30, 2026