DELTA

Primary DI
07613327547450
Brand
DELTA
Company
Stryker Leibinger GmbH & Co. KG
Model
75-72229
Catalog number
75-72229
Device description
Delta wide-fit screwdriver blade
Published
2024-09-19
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Product Codes#

Code, Name table
CodeName
HRSPlate, fixation, bone
HWCScrew, fixation, bone
MAIFastener, fixation, biodegradable, soft tissue

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HRSPlate, Fixation, BoneOrthopedic2
HWCScrew, Fixation, BoneOrthopedic2
MAIFastener, Fixation, Biodegradable, Soft TissueOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K993061000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K993061000STRYKER LEIBINGER RESORBABLE FIXATION SYSTEMStryker Instruments1999-11-19MAI

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
07613327547450PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
07613327547450076133275474507613327547450

GMDN Terms#

Term, Definition table
TermDefinition
Surgical screwdriver, reusableA non-powered tool intended to fit into a screw head (e.g., slotted, cross/hex head) for the application of rotation to introduce/remove a screw (e.g., craniofacial bone screw, dental screw) into/from a patient in association with a surgical procedure [e.g., orthopaedic, dental, computer assisted surgery (CAS), image registration]. It may also be used to connect/disconnect a device to/from another device attached to a patient (e.g., implant component, fiducial marker). The proximal end of the device may have a handle for manual use or a profiled tang that fits into an independent chuck or power driver; it is typically made of metallic and/or polymer materials. This is a reusable device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0
Length80Millimeter

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
316153956
Device count
1
Lot or batch
true
Manufacturing date on label
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
07613327694482DELTA70-9234570-923452026-07-21
07613327694499DELTA70-9235070-923502026-07-21
04546540356703NA62-2350162-235012016-12-08
04546540356710NA64-0017564-001752016-12-08
04546540356727NA64-0017664-001762016-12-08
04546540366818NA62-9202362-920232016-10-19
07613154184026NA62-0031662-003162016-12-08
07613154185450NA62-0031562-003152016-12-08
04546540246974NA60-1548660-154862016-08-24
04546540246981NA60-1549660-154962016-08-24
04546540251862NA60-8014260-801422016-08-24
04546540287168NA6514-4-1806514-4-1802016-12-08
04546540356499NA60-1600560-160052016-08-24
04546540356505NA60-1600760-160072016-08-24
04546540356512NA60-1603560-160352016-08-24
04546540356529NA60-1605060-160502016-08-24
04546540356536NA60-1903560-190352016-08-24
04546540356543NA60-2005060-200502016-08-24
04546540356567NA60-9412060-941202016-08-24
04546540356628NA62-0030262-003022016-12-08

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Primary DI, Brand, Company table
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00841731140432ARTEMIS FUZEVILEX LLCHWC2026-07-22
00841731140449ARTEMIS FUZEVILEX LLCHWC2026-07-22
00841731140456ARTEMIS FUZEVILEX LLCHWC2026-07-22
00841731140463ARTEMIS FUZEVILEX LLCHWC2026-07-22
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00841731140487ARTEMIS FUZEVILEX LLCHWC2026-07-22
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00841731140500ARTEMIS FUZEVILEX LLCHWC2026-07-22
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