← Back to catalogue

Arsenal

FDA UDI

Class II (US FDA UDI)

by Alphatec Spine, Inc.

Identity

Trade Name
Arsenal FDA UDI
Generic Name
Bone-screw internal spinal fixation system hook FDA UDI
Device Name
NARROW BLADE THORACIC SUPRALAMINAR HOOK, 8.5mm FDA UDI
Model / Reference
48600-018-085 FDA UDI
Description
NARROW BLADE THORACIC SUPRALAMINAR HOOK, 8.5mm FDA UDI

Identifiers

Primary DI / UDI-DI
00840967162690 FDA UDI
510(k) Number
K161363 FDA UDI
FDA Product Code
OSH FDA UDI
KWP FDA UDI
MNH FDA UDI
NKB FDA UDI
MNI FDA UDI
GMDN Term
Bone-screw internal spinal fixation system hook FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
888.3050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone-screw internal spinal fixation system hook

Arsenal by Alphatec 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 hook.

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

Sources (1)

  • FDA UDI 990489e0-7ecf-4d0c-b21a-69f41b5a72ad 35 fields · synced Jun 8, 2026