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Jazz Spinal System

FDA UDI

Class II (US FDA UDI)

by Implanet

Identity

Trade Name
Jazz Spinal System FDA UDI
Generic Name
Bone-screw internal spinal fixation system rod FDA UDI
Device Name
Straight rod 5.5x80 FDA UDI
Model / Reference
631337 FDA UDI
Description
Straight rod 5.5x80 FDA UDI

Identifiers

Primary DI / UDI-DI
03607506313374 FDA UDI
510(k) Number
K240392 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Bone-screw internal spinal fixation system rod FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
Commercial Distribution
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

Category: Bone-screw internal spinal fixation system rod

Jazz Spinal System by Implanet — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-screw internal spinal fixation system rod.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Implanet

Sources (1)

  • FDA UDI 4f06e90c-2b35-460f-a803-c46c6f1f1d0d 34 fields · synced Jun 8, 2026