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Invictus

FDA UDI

Class II (US FDA UDI)

by Alphatec Spine, Inc.

Identity

Trade Name
Invictus FDA UDI
Generic Name
Bone-screw internal spinal fixation system hook FDA UDI
Device Name
Pedicle Hook, 9.5 mm FDA UDI
Model / Reference
15561-095 FDA UDI
Description
Pedicle Hook, 9.5 mm FDA UDI

Identifiers

Primary DI / UDI-DI
00190376166384 FDA UDI
510(k) Number
K181677 FDA UDI
FDA Product Code
NKB FDA UDI
KWP 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

Dimensions & Sizes

Size
Height — 9.5 Millimeter FDA UDI

Category: Bone-screw internal spinal fixation system hook

Invictus 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

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Manufacturer

Sources (1)

  • FDA UDI f3bcc27c-0b15-4931-b33a-d2a04f76c9e9 36 fields · synced Jun 8, 2026