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Navagio

FDA UDI

Class II (US FDA UDI)

by Kalitec Direct LLC

Identity

Trade Name
Navagio FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
Lumbar Cage, 36x13mm 14-Degree AP CRV FDA UDI
Model / Reference
30-TEA-3613 FDA UDI
Description
Lumbar Cage, 36x13mm 14-Degree AP CRV FDA UDI

Identifiers

Catalog Number
30-TEA-3613 FDA UDI
Primary DI / UDI-DI
B07330TEA36130 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Polymeric spinal interbody fusion cage 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

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Polymeric spinal interbody fusion cage

Navagio by Kalitec Direct LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polymeric spinal interbody fusion cage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kalitec Direct LLC

Sources (1)

  • FDA UDI ab9da3a1-7099-4878-a26d-66463ae5016f 34 fields · synced Jun 6, 2026