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PRECICE® Intramedullary Limb Lengthening System

FDA UDI

Class II (US FDA UDI)

by NuVasive Specialized Orthopedics, Inc.

Identity

Trade Name
PRECICE® Intramedullary Limb Lengthening System FDA UDI
Generic Name
Portable computer FDA UDI
Device Name
ERC 2P Laptop Assembly EU FDA UDI
Model / Reference
ERC2P-LAPTOP_P_EU FDA UDI
Description
ERC 2P Laptop Assembly EU FDA UDI

Identifiers

Catalog Number
ERC2P-LAPTOP_P_EU FDA UDI
Primary DI / UDI-DI
00887517969118 FDA UDI
510(k) Number
K131490 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Portable computer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Portable computer

PRECICE® Intramedullary Limb Lengthening System by NuVasive Specialized Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Portable computer.

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 f5f69cb2-935d-48ec-b9a9-b7c5d404008b 37 fields · synced May 31, 2026