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RIVA Posterior Fixation System

FDA UDI

Class II (US FDA UDI)

by Xenix Medical

Identity

Trade Name
RIVA Posterior Fixation System FDA UDI
Generic Name
Spinal bone set screw FDA UDI
Device Name
SET SCREW, T30 FDA UDI
Model / Reference
FG1-10-000015 FDA UDI
Description
SET SCREW, T30 FDA UDI

Identifiers

Catalog Number
FG1-10-000015 FDA UDI
Primary DI / UDI-DI
00840493413624 FDA UDI
510(k) Number
K251154 FDA UDI
FDA Product Code
NKB FDA UDI
KWQ FDA UDI
OLO FDA UDI
GMDN Term
Spinal bone set screw FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
888.3060 FDA UDI
882.4560 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 set screw

RIVA Posterior Fixation System by Xenix Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal bone set screw.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Xenix Medical

Sources (1)

  • FDA UDI 781f294c-8b0f-497f-b622-3fc8d9dabd17 35 fields · synced May 30, 2026