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Transition

FDA UDI

Class II (US FDA UDI)

by Globus Medical, Inc.

Identity

Trade Name
TRANSITION FDA UDI
Generic Name
Trans-facet-screw internal spinal fixation system, sterile FDA UDI
Device Name
TRANSITION 1 Level Implant, Straight, 20mm FDA UDI
Model / Reference
152.140S FDA UDI
Description
TRANSITION 1 Level Implant, Straight, 20mm FDA UDI

Identifiers

Primary DI / UDI-DI
00849044023862 FDA UDI
510(k) Number
K073439 FDA UDI
FDA Product Code
NQP FDA UDI
GMDN Term
Trans-facet-screw internal spinal fixation system, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 20 Millimeter FDA UDI
Outer Diameter — 5.5 Millimeter FDA UDI

Category: Trans-facet-screw internal spinal fixation system, sterile

Transition by Globus Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Trans-facet-screw internal spinal fixation system, sterile.

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 302c76f5-0e6e-42e6-a2da-915a3ac01e1b 36 fields · synced May 30, 2026