← Back to catalogue

Fusion Lateral Instrument Set

FDA UDI

Class I (US FDA UDI)

by Rti Surgical, Inc.

Identity

Trade Name
Fusion Lateral Instrument Set FDA UDI
Generic Name
General internal orthopaedic fixation system implantation kit FDA UDI
Device Name
FUSION, 15in DBL SIDED RASP, 5mmx8mm FDA UDI
Model / Reference
723-553 FDA UDI
Description
FUSION, 15in DBL SIDED RASP, 5mmx8mm FDA UDI

Identifiers

Catalog Number
723-553 FDA UDI
Primary DI / UDI-DI
00191083027166 FDA UDI
FDA Product Code
HTR FDA UDI
GMDN Term
General internal orthopaedic fixation system implantation kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

Yes

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: General internal orthopaedic fixation system implantation kit

Fusion Lateral Instrument Set by Rti Surgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General internal orthopaedic fixation system implantation kit.

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
Rti Surgical, Inc.

Sources (1)

  • FDA UDI f9efaa4f-7f90-4a24-8ed7-4e1a787c312d 35 fields · synced May 31, 2026