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EIT PLIF cage

FDA UDI

Class II (US FDA UDI)

by EIT Emerging Implant Technologies GmbH

Identity

Trade Name
EIT PLIF cage FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
EIT PLIF, H 15mm, 6°, 22/9 FDA UDI
Model / Reference
PUI61502 FDA UDI
Description
EIT PLIF, H 15mm, 6°, 22/9 FDA UDI

Identifiers

Primary DI / UDI-DI
04260557779217 FDA UDI
510(k) Number
K170503 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Metallic spinal interbody fusion cage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

EIT PLIF cage by EIT Emerging Implant Technologies GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K170503 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
EIT Emerging Implant Technologies GmbH

Sources (1)

  • FDA UDI c30ef3c9-53af-4e46-b79c-6ab20a4e4852 35 fields · synced Jun 8, 2026