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S-Wire

FDA UDI

Class II (US FDA UDI)

by Spinal Resources Inc

Identity

Trade Name
S-Wire FDA UDI
Generic Name
Orthopaedic bone wire FDA UDI
Device Name
K-Wire, Single-Trocar, Round Smooth, 1.6 x 500 mm (Nitinol) FDA UDI
Model / Reference
NSTS16-500 FDA UDI
Description
K-Wire, Single-Trocar, Round Smooth, 1.6 x 500 mm (Nitinol) FDA UDI

Identifiers

Primary DI / UDI-DI
B515NSTS165000 FDA UDI
510(k) Number
K152662 FDA UDI
FDA Product Code
HTY FDA UDI
GMDN Term
Orthopaedic bone wire FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 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

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

Category: Orthopaedic bone wire

S-Wire by Spinal Resources Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone wire.

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 0e0ebf3e-c182-4f95-a35d-c0f0da7de412 34 fields · synced Jun 1, 2026