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Cavetto

FDA UDI

Class II (US FDA UDI)

by Neurostructures, Inc

Identity

Trade Name
Cavetto FDA UDI
Generic Name
General internal orthopaedic fixation system implantation kit FDA UDI
Device Name
Trial With Handle 12x14x07 FDA UDI
Model / Reference
30-90-006-121407 FDA UDI
Description
Trial With Handle 12x14x07 FDA UDI

Identifiers

Primary DI / UDI-DI
00841508105299 FDA UDI
FDA Product Code
ODP FDA UDI
GMDN Term
General internal orthopaedic fixation system implantation kit 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: General internal orthopaedic fixation system implantation kit

Cavetto by Neurostructures, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General internal orthopaedic fixation system implantation kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neurostructures, Inc

Sources (1)

  • FDA UDI 0770b053-a281-45fe-9a44-671e1189e35e 34 fields · synced Jun 1, 2026