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Precice®

FDA UDI

Class II (US FDA UDI)

by NuVasive Specialized Orthopedics, Inc.

Identity

Trade Name
Precice® FDA UDI
Generic Name
Arthrodesis intramedullary nail, magnetic distraction FDA UDI
Device Name
6.0mmx90mm Locking Screw, PT FDA UDI
Model / Reference
STP6-900-A FDA UDI
Description
6.0mmx90mm Locking Screw, PT FDA UDI

Identifiers

Primary DI / UDI-DI
00887517024978 FDA UDI
510(k) Number
K200430 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Arthrodesis intramedullary nail, magnetic distraction FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Precice® by NuVasive Specialized Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K200430 also covers:

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 c3bd943b-e48c-4aa1-a3a8-4d1be64f6796 36 fields · synced May 31, 2026