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Matrix

FDA UDI

Class II (US FDA UDI)

by Synthes

Identity

Trade Name
Matrix FDA UDI
Generic Name
Spinal bone screw head/rod adaptor FDA UDI
Device Name
TI MATRIX TOP LOADING POLYAXIAL HEAD FDA UDI
Model / Reference
04.632.001 FDA UDI
Description
TI MATRIX TOP LOADING POLYAXIAL HEAD FDA UDI

Identifiers

Catalog Number
04632001 FDA UDI
Primary DI / UDI-DI
10705034744971 FDA UDI
FDA Product Code
MNH FDA UDI
KWP FDA UDI
KWQ FDA UDI
NKB FDA UDI
MNI FDA UDI
GMDN Term
Spinal bone screw head/rod adaptor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
888.3050 FDA UDI
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 bone screw head/rod adaptor

Matrix by Synthes — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal bone screw head/rod adaptor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Synthes

Sources (1)

  • FDA UDI 95c45356-3c20-45d0-9c3a-f5ba67dc29a0 35 fields · synced May 31, 2026