FDA.report

INFINITY™ Occipitocervical Upper Thoracic System

Primary DI
00763000990848
Brand
INFINITY™ Occipitocervical Upper Thoracic System
Company
MEDTRONIC SOFAMOR DANEK, INC.
Model
3653536
Device description
RMAS FT 3653536 3.5MM SCREW 3.5X36MM
Published
2026-03-22
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
MR Conditional
Rx
true
OTC
false
Sterile
false
Single use
true

Related Records

Product Codes

CodeName
NKGPosterior cervical screw system

Product Code Classifications

CodeDeviceSpecialtyClass
NKGPosterior Cervical Screw SystemOrthopedic2

Premarket Submissions

SubmissionSupplement
K253129000

Premarket Details

SubmissionSupplementDeviceApplicantDecision dateProduct code
K253129000Infinity™ OCT SystemMedtronic Sofamor Danek USA, Inc.2025-10-24NKG

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00763000990848PrimaryGS10

GMDN Terms

TermDefinition
Spinal bone screw, non-bioabsorbableA small, threaded, implantable rod with a screw head and drive intended for internal spinal fixation by being screwed into the spine to hold a correction/stabilization device (e.g., rod, plate, tether) to bone; it is made of a material that is not chemically degraded or absorbed via natural body processes (e.g., surgical steel, titanium alloy, carbon fibre). It is available in various types (e.g., pedicle or transfacet, with a slotted, cross, star, or polygonal drive), and is typically used to provide immobilization and stabilization of spinal segments in the treatment of spinal instabilities or deformities. A screw head adaptor intended to stabilize a rod may be included with the screw.

Sterilization Methods

Method
Moist Heat or Steam Sterilization

Contacts

PhoneEmail
+1(800)633-8766Corporate.UDI@medtronic.com

Regulatory Flags

DUNS number
830350380
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

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00763000869076CD HORIZON® Spinal System593290152026-03-21
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00763000869106CD HORIZON® Spinal System593290182026-03-21

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