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HiJAK™ Cervical

FDA UDI

Class II (US FDA UDI)

by Atlas Spine Inc.

Identity

Trade Name
HiJAK™ Cervical FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
Driver, LG, HiJAK ™ Cervical FDA UDI
Model / Reference
2019-01-0003 FDA UDI
Description
Driver, LG, HiJAK ™ Cervical FDA UDI

Identifiers

Catalog Number
2019-01-0003 FDA UDI
Primary DI / UDI-DI
M68120190100030 FDA UDI
510(k) Number
K180675 FDA UDI
FDA Product Code
ODP FDA UDI
GMDN Term
Surgical screwdriver, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Surgical screwdriver, reusable

HiJAK™ Cervical by Atlas Spine Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical screwdriver, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Atlas Spine Inc.

Sources (1)

  • FDA UDI 4bf8639a-7fe8-4acb-be87-d0f1a141a74e 36 fields · synced Jun 1, 2026