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PreView II™

FDA UDI

Class II (US FDA UDI)

by Nexus Spine, L.l.c.

Identity

Trade Name
PreView II™ FDA UDI
Generic Name
Spinal fixation plate, non-bioabsorbable FDA UDI
Device Name
ACP 3 Level x 51 mm, Swivel Lock FDA UDI
Model / Reference
521167 FDA UDI
Description
ACP 3 Level x 51 mm, Swivel Lock FDA UDI

Identifiers

Primary DI / UDI-DI
B6785211670 FDA UDI
510(k) Number
K062371 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

Dimensions & Sizes

Size
Length — 51 Millimeter FDA UDI

Category: Spinal fixation plate, non-bioabsorbable

PreView II™ by Nexus Spine, L.l.c. — 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
Nexus Spine, L.l.c.

Sources (1)

  • FDA UDI 5e923a9e-34c5-47f0-b36f-72720351c9ba 35 fields · synced May 31, 2026