FDA.reportPublic FDA data

KHEIRON

Primary DI
03701313009595
Brand
KHEIRON
Company
S.M.A.I.O
Model
30KR55004
Device description
Ø5.5 Ti K-ROD for DePuy Synthes
Published
2026-01-27
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Product Codes#

Code, Name table
CodeName
KWPAppliance, Fixation, Spinal Interlaminal
NKBThoracolumbosacral Pedicle Screw System

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KWPAppliance, Fixation, Spinal InterlaminalOrthopedic2
NKBThoracolumbosacral Pedicle Screw SystemOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K253990000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K253990000KHEIRON® Spinal Fixation System, including patient specific K-RODS.M.A.I.O2026-01-07NKB

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
03701313009595PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
03701313009595037013130095953701313009595

GMDN Terms#

Term, Definition table
TermDefinition
Bone-screw internal spinal fixation system rodAn implantable component of a bone-screw internal spinal fixation system in the form of a thin cylinder intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, and also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. This component is designed as a longitudinal (intervertebral) connecting element passing through the system’s implantable screw heads or hooks. It is available in various forms (e.g., straight, curved, rigid, flexible, with varying diameters); flexible types may allow small movements of the spine.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
260585710
Device count
1
DM exempt
true
Lot or batch
true
Serial number
true
Manufacturing date on label
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
03701313009618KHEIRON30KR550022026-09-23
03701313009502K-ROD01TR200002026-09-22
03701313007935KBA3DV2.0.02023-07-24
03701313000479KBA3DV1.1.X2023-06-05
03701313009526KHEIRON01PR20302026-07-06
03701313009519KHEIRON01PR20202026-07-05
03701313005177KHEIRON29TC6030229TC603022024-06-24
03701313005184KHEIRON29TC6030129TC603012024-06-24
03701313005191KHEIRON29TC6020229TC602022024-06-24
03701313005207KHEIRON29TC6020129TC602012024-06-24
03701313005214KHEIRON29TC6010229TC601022024-06-24
03701313005221KHEIRON29TC6010129TC601012024-06-24
03701313005238KHEIRON29TC5530229TC553022024-06-24
03701313005245KHEIRON29TC5530129TC553012024-06-24
03701313005252KHEIRON29TC5520229TC552022024-06-24
03701313005269KHEIRON29TC5520129TC552012024-06-24
03701313005276KHEIRON29TC5510229TC551022024-06-24
03701313005283KHEIRON29TC5510129TC551012024-06-24
03701313000028KHEIRON24TS0293124TS029312020-12-14
03701313000035KHEIRON24TS0313524TS031352020-12-14

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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