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KYPHON® One-Step™ Osteo Introducer™ System

FDA UDI

Class I (US FDA UDI)

by Medtronic Sofamor Danek, Inc.

Identity

Trade Name
KYPHON® One-Step™ Osteo Introducer™ System FDA UDI
Generic Name
Bone access channel kit FDA UDI
Device Name
INTRODUCER T15J OIS ONE-STEP TRO AND DIA FDA UDI
Model / Reference
T15J FDA UDI
Description
INTRODUCER T15J OIS ONE-STEP TRO AND DIA FDA UDI

Identifiers

Primary DI / UDI-DI
00643169097216 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Bone access channel kit 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Category: Bone access channel kit

KYPHON® One-Step™ Osteo Introducer™ System by Medtronic Sofamor Danek, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone access channel kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 76c3c157-f26f-47e4-a70b-62d2bbb6b90a 34 fields · synced Jun 8, 2026