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Songer® Spinal Cable System

FDA UDI

Class II (US FDA UDI)

by Pioneer Surgical Technology, Inc.

Identity

Trade Name
Songer® Spinal Cable System FDA UDI
Generic Name
Internal spinal fixation system cable FDA UDI
Device Name
(1) Ø1.25mm Cable, Double Loop with Crimp, (2) Crimp, Flange FDA UDI
Model / Reference
400-201 FDA UDI
Description
(1) Ø1.25mm Cable, Double Loop with Crimp, (2) Crimp, Flange FDA UDI

Identifiers

Catalog Number
7925-011S FDA UDI
Primary DI / UDI-DI
00840298704583 FDA UDI
510(k) Number
K941213 FDA UDI
FDA Product Code
JDQ FDA UDI
GMDN Term
Internal spinal fixation system cable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3010 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Internal spinal fixation system cable

Songer® Spinal Cable System by Pioneer Surgical Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Internal spinal fixation system cable.

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 226da5f0-74c3-4e85-b514-13fe5ac42bd5 36 fields · synced Jun 6, 2026