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Vault C ACDF System

FDA UDI

Class II (US FDA UDI)

by Precision Spine, Inc.

Identity

Trade Name
Vault C ACDF System FDA UDI
Generic Name
Spinal fixation plate, non-bioabsorbable FDA UDI
Device Name
14 x 12 x 07mm Anterior Plate FDA UDI
Model / Reference
37-PA-4207 FDA UDI
Description
14 x 12 x 07mm Anterior Plate FDA UDI

Identifiers

Catalog Number
37-PA-4207 FDA UDI
Primary DI / UDI-DI
00840019903837 FDA UDI
510(k) Number
K132029 FDA UDI
FDA Product Code
OVE FDA UDI
GMDN Term
Spinal fixation plate, non-bioabsorbable 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

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

No

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: Spinal fixation plate, non-bioabsorbable

Vault C ACDF System by Precision 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

Sources (1)

  • FDA UDI 1776e41b-8bfa-430f-bde1-7867c65c867a 35 fields · synced May 30, 2026