← Back to catalogue

TRIALTIS Spine System

FDA UDI

Class II (US FDA UDI)

by Depuy Spine, Inc.

Identity

Trade Name
TRIALTIS Spine System FDA UDI
Generic Name
Bone-screw internal spinal fixation system connector FDA UDI
Device Name
TRIALTIS Spine System Open Lateral Connector Fixed, Flanged ø5.5-6mm to 6mm x 30mm FDA UDI
Model / Reference
5560636030FS FDA UDI
Description
TRIALTIS Spine System Open Lateral Connector Fixed, Flanged ø5.5-6mm to 6mm x 30mm FDA UDI

Identifiers

Catalog Number
5560636030FS FDA UDI
Primary DI / UDI-DI
10705034601601 FDA UDI
510(k) Number
K243249 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Bone-screw internal spinal fixation system connector 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Bone-screw internal spinal fixation system connector

TRIALTIS Spine System by Depuy Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-screw internal spinal fixation system connector.

Cleared under the same submission

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
Depuy Spine, Inc.

Sources (1)

  • FDA UDI 1303ee64-93e3-4275-81d4-394c089b207b 36 fields · synced Jun 8, 2026