FDA.reportPublic FDA data

Freedom Posterior Cervical Screw - Φ 4 mm, 38 mm

Primary DI
09348215087609
Brand
Freedom Posterior Cervical Screw - Φ 4 mm, 38 mm
Company
SIGNATURE ORTHOPAEDICS PTY LTD
Model
131-45-8038
Published
2026-04-30
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
NKGPosterior Cervical Screw System

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
NKGPosterior Cervical Screw SystemOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K242674000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K242674000Freedom Posterior Cervical ScrewsSignature Orthopaedics Pty, Ltd.2025-05-13NKG

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
09348215087609PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
09348215087609093482150876099348215087609

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.

Regulatory Flags#

DUNS number
751993028
Device count
1
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
09348215185428Signature Magnum Acetabular Cup111-67-00442026-07-29
09348215185435Signature Magnum Acetabular Cup111-67-00462026-07-29
09348215185442Signature Magnum Acetabular Cup111-67-00482026-07-29
09348215185459Signature Magnum Acetabular Cup111-67-00502026-07-29
09348215185466Signature Magnum Acetabular Cup111-67-00522026-07-29
09348215185473Signature Magnum Acetabular Cup111-67-00542026-07-29
09348215185480Signature Magnum Acetabular Cup111-67-00562026-07-29
09348215185497Signature Magnum Acetabular Cup111-67-00582026-07-29
09348215185503Signature Magnum Acetabular Cup111-67-00602026-07-29
09348215185510Signature Magnum Acetabular Cup111-67-00622026-07-29
09348215185527Signature Magnum Acetabular Cup111-67-00642026-07-29
09348215185534Signature Magnum Acetabular Cup111-67-00662026-07-29
09348215185541Signature Resurfacing Femoral Head111-67-01382026-07-29
09348215185558Signature Resurfacing Femoral Head111-67-01402026-07-29
09348215185565Signature Resurfacing Femoral Head111-67-01422026-07-29
09348215185572Signature Resurfacing Femoral Head111-67-01442026-07-29
09348215185589Signature Resurfacing Femoral Head111-67-01462026-07-29
09348215185596Signature Resurfacing Femoral Head111-67-01482026-07-29
09348215185602Signature Resurfacing Femoral Head111-67-01502026-07-29
09348215185619Signature Resurfacing Femoral Head111-67-01522026-07-29

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