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icotec Ant. Cervical Plate, 3 Segmental, 73 mm

FDA UDI

Class II (US FDA UDI)

by Icotec

Identity

Trade Name
icotec Ant. Cervical Plate, 3 Segmental, 73 mm FDA UDI
Generic Name
Spinal fixation plate, non-bioabsorbable FDA UDI
Device Name
icotec Ant. Cervical Plate, 3 Segmental, 73 mm FDA UDI
Model / Reference
12-73-18-73 FDA UDI
Description
icotec Ant. Cervical Plate, 3 Segmental, 73 mm FDA UDI

Identifiers

Primary DI / UDI-DI
07640140438368 FDA UDI
FDA Product Code
KWQ FDA UDI
GMDN Term
Spinal fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 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: Spinal fixation plate, non-bioabsorbable

icotec Ant. Cervical Plate, 3 Segmental, 73 mm by Icotec — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal fixation plate, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Icotec

Sources (1)

  • FDA UDI d86819d3-09f1-40d6-b49f-b8a36ad0b31c 34 fields · synced May 30, 2026