FDA.reportPublic FDA data

ASTER

Primary DI
08800071055464
Brand
ASTER
Company
OSTEONIC CO.,Ltd.
Model
N3A.20210
Device description
1Level, 21mm (H to H 12mm)
Published
2026-04-27
Public version status
New
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
KWQAppliance, fixation, spinal intervertebral body

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KWQAppliance, Fixation, Spinal Intervertebral BodyOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K254182000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K254182000AsterOsteonic Co., Ltd.2026-02-26KWQ

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
08800071055464PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08800071055464088000710554648800071055464

GMDN Terms#

Term, Definition table
TermDefinition
Spinal fixation plate, non-bioabsorbableA small, implantable, non-customized sheet of solid material intended to be attached to the spine with screws for spinal immobilization as part of treatment of a spinal instability or deformity; it is made of a material that is not chemically degraded or absorbed via natural body processes (includes implant grade metal such as surgical steel, titanium alloy, or carbon fibre). Disposable instruments intended to facilitate implantation, or fixation implants (i.e., bone screws), may be packaged with the plate.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+821041480931yjlim@osteonic.com

Regulatory Flags#

DUNS number
688999370
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
08800071055471ASTERN3A.202302026-05-18
08800071055457ASTERN3A.201902026-04-27
08800071055440ASTERN3A.201702026-03-19
08809416064703SignexA2C.080702025-06-24
08809416064802SignexA1R.080102025-06-24
08809416065267SignexA2A.100502025-06-24
08809416065274SignexA2A.100802025-06-24
08809416065281SignexA2B.100802025-06-24
08809416065298SignexA2C.100502025-06-24
08809416065410SignexA2A.130502025-06-24
08809595977733SignexA2A.080402025-06-24
08809595977740SignexA2A.080602025-06-24
08809595977757SignexA2A.081202025-06-24
08809595977764SignexA2A.100402025-06-24
08809595977818SignexA2B.080802025-06-24
08809595977832SignexA2C.080602025-06-24
08809416064581SignexA1A.060402025-07-01
08809416064598SignexA1A.061202025-07-01
08809416064604SignexA1C.060702025-07-01
08809416064611SignexA1E.060702025-07-01

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
08809986492791CastleLoc-P Anterior Cervical Plate SystemL&K BIOMED CO. ,LTD.KWQ2026-06-09
08809986492807CastleLoc-P Anterior Cervical Plate SystemL&K BIOMED CO. ,LTD.KWQ2026-06-09
08809986492814CastleLoc-P Anterior Cervical Plate SystemL&K BIOMED CO. ,LTD.KWQ2026-06-09
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00840493423265RIVA Pedicle Screw SystemXENIX MEDICAL LLCKWQ2026-06-08
00840493423272RIVA Pedicle Screw SystemXENIX MEDICAL LLCKWQ2026-06-08
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00840493423340RIVA Pedicle Screw SystemXENIX MEDICAL LLCKWQ2026-06-08
00840493423357RIVA Pedicle Screw SystemXENIX MEDICAL LLCKWQ2026-06-08
00840493423364RIVA Pedicle Screw SystemXENIX MEDICAL LLCKWQ2026-06-08
00840493423371RIVA Pedicle Screw SystemXENIX MEDICAL LLCKWQ2026-06-08
00840493423388RIVA Pedicle Screw SystemXENIX MEDICAL LLCKWQ2026-06-08
00840493423395RIVA Pedicle Screw SystemXENIX MEDICAL LLCKWQ2026-06-08
00840493423401RIVA Pedicle Screw SystemXENIX MEDICAL LLCKWQ2026-06-08
00840493423418RIVA Pedicle Screw SystemXENIX MEDICAL LLCKWQ2026-06-08
00840493423425RIVA Pedicle Screw SystemXENIX MEDICAL LLCKWQ2026-06-08