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KYPHON Express II Inflatable Bone Tamp

FDA UDI

Class II (US FDA UDI)

by Medtronic Sofamor Danek, Inc.

Identity

Trade Name
KYPHON Express II Inflatable Bone Tamp FDA UDI
Generic Name
Inflatable bone tamp FDA UDI
Device Name
BONE TAMP KE202 20/2 EXPRESS II IBT FDA UDI
Model / Reference
KE202 FDA UDI
Description
BONE TAMP KE202 20/2 EXPRESS II IBT FDA UDI

Identifiers

Primary DI / UDI-DI
00763000312053 FDA UDI
510(k) Number
K123771 FDA UDI
FDA Product Code
HRX FDA UDI
HXG FDA UDI
GMDN Term
Inflatable bone tamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 FDA UDI
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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Inflatable bone tamp

KYPHON Express II Inflatable Bone Tamp by Medtronic Sofamor Danek, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Inflatable bone tamp.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cda5d242-1bac-46b7-b8ab-858e9e257e30 36 fields · synced May 30, 2026