← Back to catalogue

icotec Cervical Cage Anatomic 7 x 13 mm

FDA UDI

Class II (US FDA UDI)

by Icotec

Identity

Trade Name
icotec Cervical Cage Anatomic 7 x 13 mm FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
icotec Cervical Cage Anatomic 7 x 13 mm FDA UDI
Model / Reference
13-41-0713 FDA UDI
Description
icotec Cervical Cage Anatomic 7 x 13 mm FDA UDI

Identifiers

Catalog Number
13-41-0713 FDA UDI
Primary DI / UDI-DI
07640164847948 FDA UDI
FDA Product Code
MAX FDA UDI
ODP 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

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

No

FDA UDI

Category: Polymeric spinal interbody fusion cage

icotec Cervical Cage Anatomic 7 x 13 mm by Icotec — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Icotec

Sources (1)

  • FDA UDI 97343a92-93db-4501-ad22-0da749bdf10e 35 fields · synced May 30, 2026