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Paeon Anterior Cervical Plate System

FDA UDI

Class II (US FDA UDI)

by Aegis Spine, Inc.

Identity

Trade Name
Paeon Anterior Cervical Plate System FDA UDI
Generic Name
Spinal fixation plate, non-bioabsorbable FDA UDI
Device Name
Cervical Plate Contour Type 3 Level 60mm FDA UDI
Model / Reference
6713-1760S FDA UDI
Description
Cervical Plate Contour Type 3 Level 60mm FDA UDI

Identifiers

Catalog Number
6713-1760S FDA UDI
Primary DI / UDI-DI
00840273300229 FDA UDI
510(k) Number
K210035 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

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 fixation plate, non-bioabsorbable

Paeon Anterior Cervical Plate System by Aegis Spine, Inc. — 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
Aegis Spine, Inc.

Sources (1)

  • FDA UDI ed9bcf41-e58f-4e92-a4f3-9f0332bb5e11 35 fields · synced May 31, 2026