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YUKON OCT Spinal System

FDA UDI

Class II (US FDA UDI)

by K2m, Inc.

Identity

Trade Name
YUKON OCT Spinal System FDA UDI
Generic Name
Bone-screw internal spinal fixation system connector FDA UDI
Device Name
Parallel Connector, Closed Size Ø3.5/4.0 mm, 4 Scr FDA UDI
Model / Reference
7601-83535A-G1 FDA UDI
Description
Parallel Connector, Closed Size Ø3.5/4.0 mm, 4 Scr FDA UDI

Identifiers

Catalog Number
7601-83535A-G1 FDA UDI
Primary DI / UDI-DI
10888857396807 FDA UDI
FDA Product Code
NKG FDA UDI
KWP FDA UDI
GMDN Term
Bone-screw internal spinal fixation system connector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3075 FDA UDI
888.3050 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

Dimensions & Sizes

Size
Outer Diameter — 3.5 Millimeter FDA UDI

Category: Bone-screw internal spinal fixation system connector

YUKON OCT Spinal System by K2m, 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
K2m, Inc.

Sources (1)

  • FDA UDI 04b6a764-cd07-41cc-b0ca-c2feed10d2ae 36 fields · synced May 31, 2026