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PRECICE Bone Transport

FDA UDI

Class I (US FDA UDI)

by NuVasive Specialized Orthopedics, Inc.

Identity

Trade Name
PRECICE Bone Transport FDA UDI
Generic Name
Surgical implant template, single-use FDA UDI
Device Name
Bone Transport Bent Trial Nail FDA UDI
Model / Reference
BTB1-000 FDA UDI
Description
Bone Transport Bent Trial Nail FDA UDI

Identifiers

Primary DI / UDI-DI
00887517012364 FDA UDI
FDA Product Code
HWT FDA UDI
GMDN Term
Surgical implant template, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Surgical implant template, single-use

PRECICE Bone Transport by NuVasive Specialized Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical implant template, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
NuVasive Specialized Orthopedics, Inc.

Sources (1)

  • FDA UDI 44a39054-9ae9-45c0-88bc-8854698896dd 33 fields · synced Jun 6, 2026