← Back to catalogue

VADER Pedicle System, Parallel Connector, Closed, Ø 6.0 mm - Ø 6.0 mm

FDA UDI

Class II (US FDA UDI)

by Icotec

Identity

Trade Name
VADER Pedicle System, Parallel Connector, Closed, Ø 6.0 mm - Ø 6.0 mm FDA UDI
Generic Name
Bone-screw internal spinal fixation system connector FDA UDI
Device Name
VADER Pedicle System, Parallel Connector, Closed, Ø 6.0 mm - Ø 6.0 mm FDA UDI
Model / Reference
16-6060-0225 FDA UDI
Description
VADER Pedicle System, Parallel Connector, Closed, Ø 6.0 mm - Ø 6.0 mm FDA UDI

Identifiers

Catalog Number
16-6060-0225 FDA UDI
Primary DI / UDI-DI
07640172552865 FDA UDI
FDA Product Code
NKB FDA UDI
PML FDA UDI
GMDN Term
Bone-screw internal spinal fixation system connector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
888.3027 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

Category: Bone-screw internal spinal fixation system connector

VADER Pedicle System, Parallel Connector, Closed, Ø 6.0 mm - Ø 6.0 mm by Icotec — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-screw internal spinal fixation system connector.

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

Manufacturer
Icotec

Sources (1)

  • FDA UDI fcb0b522-dcd1-4f5a-b3e5-b67f527ee097 35 fields · synced May 30, 2026