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Neo Pedicle Screw System

FDA UDI

Class II (US FDA UDI)

by Neo Medical Inc.

Identity

Trade Name
Neo Pedicle Screw System FDA UDI
Generic Name
Spinal bone screw, non-bioabsorbable FDA UDI
Device Name
Iliac screw Ø8.0 x 100mm FDA UDI
Model / Reference
SC-80-10-IL FDA UDI
Description
Iliac screw Ø8.0 x 100mm FDA UDI

Identifiers

Primary DI / UDI-DI
07640177820747 FDA UDI
510(k) Number
K212489 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Spinal bone screw, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 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
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 8 Millimeter FDA UDI
Length — 100 Millimeter FDA UDI

Category: Spinal bone screw, non-bioabsorbable

Neo Pedicle Screw System by Neo Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal bone screw, 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
Neo Medical Inc.

Sources (1)

  • FDA UDI 50bcb736-e57b-4d80-a124-25a9c467d8da 36 fields · synced May 29, 2026