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Elatus Lumbar Plate System

FDA UDI

Class II (US FDA UDI)

by Aegis Spine, Inc.

Identity

Trade Name
Elatus Lumbar Plate System FDA UDI
Generic Name
Spinal bone screw, non-bioabsorbable FDA UDI
Device Name
Fixed Lumbar Plate Screw Cancellous Ø 5.5x 45mm FDA UDI
Model / Reference
7101-5545S FDA UDI
Description
Fixed Lumbar Plate Screw Cancellous Ø 5.5x 45mm FDA UDI

Identifiers

Catalog Number
7101-5545S FDA UDI
Primary DI / UDI-DI
00840273302438 FDA UDI
510(k) Number
K210035 FDA UDI
FDA Product Code
KWQ FDA UDI
GMDN Term
Spinal bone screw, 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

No

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: Spinal bone screw, non-bioabsorbable

Elatus Lumbar Plate System by Aegis Spine, 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
Aegis Spine, Inc.

Sources (1)

  • FDA UDI a6ca243e-a084-4432-ae5c-1044a589298d 35 fields · synced May 31, 2026