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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 pin, non-bioabsorbable FDA UDI
Device Name
K-Wire, Double-Round Smooth, 1.6 x 500 mm (Nitinol) FDA UDI
Model / Reference
NDRS16-500 FDA UDI
Description
K-Wire, Double-Round Smooth, 1.6 x 500 mm (Nitinol) FDA UDI

Identifiers

Primary DI / UDI-DI
B515NDRS165000 FDA UDI
510(k) Number
K152662 FDA UDI
FDA Product Code
HTY FDA UDI
GMDN Term
Orthopaedic bone pin, non-bioabsorbable 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

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

Category: Orthopaedic bone pin, non-bioabsorbable

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 pin, non-bioabsorbable.

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 14073227-8358-46d6-8d43-544696b35490 34 fields · synced May 30, 2026