FDA.reportPublic FDA data

CD HORIZON® Fenestrated Screw Set

Primary DI
00643169679177
Brand
CD HORIZON® Fenestrated Screw Set
Company
MEDTRONIC SOFAMOR DANEK, INC.
Model
55840029550T
Device description
MAS 55840029550T 5.5/6.0 FENSTRTD 9.5X50
Published
2016-04-09
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
MNIORTHOSIS, SPINAL PEDICLE FIXATION

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MNIOrthosis, Spinal Pedicle FixationOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K152604000
K193011000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K152604000KYPHON HV-R Fenestrated Screw Cement, CD HORIZON Fenestrated Screw SetMedtronic Sofamor Danek USA, Incorporated2016-01-06PML
K193011000CD Horizon™ Fenestrated Screw SetMedtronic Sofamor Danek USA, Inc.2020-01-10NKB

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00643169679177PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00643169679177006431696791776431696791770643169679177

GMDN Terms#

Term, Definition table
TermDefinition
Bone-screw internal spinal fixation system, non-sterileAn assembly of non-sterile implantable devices intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. Otherwise known as a pedicle screw instrumentation system, it typically consists of a combination of anchors (e.g., bolts, hooks, pedicle screws or other types), interconnection mechanisms (incorporating nuts, screws, sleeves, or bolts), longitudinal members (e.g., plates, rods, plate/rod combinations), and/or transverse connectors. Non-sterile disposable devices associated with implantation may be included.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Circumference9.5Millimeter
Length50Millimeter

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(800)633-8766Corporate.UDI@medtronic.com

Regulatory Flags#

DUNS number
830350380
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00763000703929MSB CAPSTONE CONTROL™ Spinal System39914222026-08-27
00763000703936MSB CAPSTONE CONTROL™ Spinal System39914272026-08-27
00763000703950MSB CAPSTONE CONTROL™ Spinal System39915222026-08-27
00763000703967MSB CAPSTONE CONTROL™ Spinal System39915272026-08-27
00763000703981MSB CAPSTONE CONTROL™ Spinal System39916222026-08-27
00763000703998MSB CAPSTONE CONTROL™ Spinal System39916272026-08-27
00763000704001MSB CAPSTONE CONTROL™ Spinal System39916322026-08-27
00763000704018MSB CAPSTONE CONTROL™ Spinal System39917222026-08-27
00763000704025MSB CAPSTONE CONTROL™ Spinal System39917272026-08-27
00763000704032MSB CAPSTONE CONTROL™ Spinal System39917322026-08-27
00763000704049MSB CAPSTONE CONTROL™ Spinal System39913322026-08-27
00763000704063MSB CAPSTONE CONTROL™ Spinal System39908272026-08-27
00763000704070MSB CAPSTONE CONTROL™ Spinal System39909222026-08-27
00763000704100MSB CAPSTONE CONTROL™ Spinal System39910272026-08-27
00763000704117MSB CAPSTONE CONTROL™ Spinal System39910322026-08-27
00763000704124MSB CAPSTONE CONTROL™ Spinal System39911222026-08-27
00763000704131MSB CAPSTONE CONTROL™ Spinal System39911272026-08-27
00763000704148MSB CAPSTONE CONTROL™ Spinal System39911322026-08-27
00763000704155MSB CAPSTONE CONTROL™ Spinal System39912222026-08-27
00763000704162MSB CAPSTONE CONTROL™ Spinal System39912272026-08-27

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00889929072943Inertia® Pedicle Screw SystemNEXXT SPINE, LLCMNI2026-08-26
M719IST80030C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80035C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80040C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80045C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80050C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80055C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80060C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80065C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80070C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80075C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80080C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80085C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80090C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80095C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80100C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80105C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80110C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80115C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80120C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80125C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80130C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80135C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80140C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80145C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719IST80150C0TiLockGenesys Orthopedics Systems LLCMNI2026-08-18
M719GSIX785D160TiLockGenesys Orthopedics Systems LLCMNI2026-08-17
M719GSIX785D210TiLockGenesys Orthopedics Systems LLCMNI2026-08-17
M719GSIX785D260TiLockGenesys Orthopedics Systems LLCMNI2026-08-17
M719GSIX785D310TiLockGenesys Orthopedics Systems LLCMNI2026-08-17