FDA.report

DENALI® Spinal System

Primary DI
10888857007635
Brand
DENALI® Spinal System
Company
K2M, INC.
Model
101-80012G-SG
Catalog number
101-80012G-SG
Device description
Lumbar Laminar Hook, Standard, Closed, Size (M)
Published
2016-11-14
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Related Records

Contact Domains

Product Codes

CodeName
OSHPedicle screw spinal system, adolescent idiopathic scoliosis

Product Code Classifications

CodeDeviceSpecialtyClass
OSHPedicle Screw Spinal System, Adolescent Idiopathic ScoliosisOrthopedic2

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
10888857007635PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalized
1088885700763510888857007635

GMDN Terms

TermDefinition
Bone-screw internal spinal fixation system, sterileAn assembly of 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. Sterile disposable devices associated with implantation may be included.

Device Sizes

TypeValueUnit
Device Size Text, specify0
Outer Diameter5.5Millimeter

Sterilization Methods

Method

Contacts

PhoneEmail
+1(703)777-3155mzellers@k2m.com
+1(571)919-2000mark.zellers@stryker.com
+1(571)919-2000christopher.tomea@stryker.com

Regulatory Flags

DUNS number
146060863
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
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

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10888857574700Q Interbody Instruments8020-90092-GS8020-90092-GS2026-03-03
10888857578715Q Interbody Instruments8020-100018020-100012026-03-03
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