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Kheiron

FDA UDI

Class II (US FDA UDI)

by S.m.a.i.o

Identity

Trade Name
KHEIRON FDA UDI
Generic Name
Bone-screw internal spinal fixation system rod FDA UDI
Device Name
Ø5.5 90° L150-150mm curved Ti rod FDA UDI
Model / Reference
24CR55915 FDA UDI
Description
Ø5.5 90° L150-150mm curved Ti rod FDA UDI

Identifiers

Catalog Number
24CR55915 FDA UDI
Primary DI / UDI-DI
03701313000097 FDA UDI
510(k) Number
K201659 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

Kheiron by S.m.a.i.o — 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

K201659 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
S.m.a.i.o

Sources (1)

  • FDA UDI 59911b3f-6b37-4404-82a2-b70da4413bfd 36 fields · synced May 30, 2026