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FortiBridge

FDA UDI

Class II (US FDA UDI)

by Nanovis Spine, Llc

Identity

Trade Name
FortiBridge FDA UDI
Generic Name
Spinal fixation plate, non-bioabsorbable FDA UDI
Device Name
FortiBridge Variable Screw 4mm x 18mm FDA UDI
Model / Reference
10703-4018 FDA UDI
Description
FortiBridge Variable Screw 4mm x 18mm FDA UDI

Identifiers

Catalog Number
10703-4018 FDA UDI
Primary DI / UDI-DI
10814216022681 FDA UDI
510(k) Number
K143706 FDA UDI
FDA Product Code
KWQ FDA UDI
GMDN Term
Spinal fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 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 — 4.0 Millimeter FDA UDI
Length — 18 Millimeter FDA UDI

Category: Spinal fixation plate, non-bioabsorbable

FortiBridge by Nanovis Spine, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal fixation plate, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nanovis Spine, Llc

Sources (1)

  • FDA UDI 5df28244-6d07-4520-bcfe-7df06b8ab118 37 fields · synced May 30, 2026