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Acp

FDA UDI

Class II (US FDA UDI)

by Nuvasive, Inc.

Identity

Trade Name
ACP FDA UDI
Generic Name
Spinal fixation plate, non-bioabsorbable FDA UDI
Device Name
ACP 2.1H Plate, 43mm 2-Level FDA UDI
Model / Reference
18002243 FDA UDI
Description
ACP 2.1H Plate, 43mm 2-Level FDA UDI

Identifiers

Primary DI / UDI-DI
00887517062086 FDA UDI
510(k) Number
K201078 FDA UDI
K203253 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

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

Yes

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

Acp by Nuvasive, 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
Nuvasive, Inc.

Sources (1)

  • FDA UDI 7adb771d-aac2-44bf-9d7b-8fd9c60ae9bb 35 fields · synced May 30, 2026