← Back to catalogue

Fusion Posterior Instrument Set

FDA UDI

Class I (US FDA UDI)

by Rti Surgical, Inc.

Identity

Trade Name
Fusion Posterior Instrument Set FDA UDI
Generic Name
Bone graft funnel FDA UDI
Device Name
FUSION, BONE GRAFT FUNNEL FDA UDI
Model / Reference
723-410 FDA UDI
Description
FUSION, BONE GRAFT FUNNEL FDA UDI

Identifiers

Catalog Number
723-410 FDA UDI
Primary DI / UDI-DI
00191083026060 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Bone graft funnel FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Bone graft funnel

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

Similar devices

Also classified as Bone graft funnel.

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 ae85c909-94af-42f7-989a-6c07b242b22c 35 fields · synced May 30, 2026