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Vectra-T

FDA UDI

Class II (US FDA UDI)

by Synthes

Identity

Trade Name
VECTRA-T FDA UDI
Generic Name
Spinal fixation plate, non-bioabsorbable FDA UDI
Device Name
TI VECTRA-T(TM) PLATE 2 LEVEL/36MM FDA UDI
Model / Reference
450.565 FDA UDI
Description
TI VECTRA-T(TM) PLATE 2 LEVEL/36MM FDA UDI

Identifiers

Catalog Number
450565 FDA UDI
Primary DI / UDI-DI
10705034782195 FDA UDI
510(k) Number
K051665 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

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: Spinal fixation plate, non-bioabsorbable

Vectra-T by Synthes — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal fixation plate, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Synthes

Sources (1)

  • FDA UDI ead86dea-0bba-48af-9170-4f5e3ff65f26 36 fields · synced Jun 8, 2026