APTUS

Primary DI
07630894821639
Brand
APTUS
Company
Medartis AG
Model
P-4031.07S
Catalog number
P-4031.07S
Device description
3.5 PentaLock Prox.Hum. Plate XL, 10H, L
Published
2026-10-27
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
HRSPlate, fixation, bone

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HRSPlate, Fixation, BoneOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K253916000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K253916000APTUS Shoulder Proximal Humerus System, PentaLock 3.5Medartis AG2026-03-16HRS

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
07630894821639PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
07630894821639076308948216397630894821639

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic fixation plate, non-bioabsorbableA non-bioabsorbable, non-customized, firm, implantable sheet intended to stabilize a fractured orthopaedic bone (excluding craniofacial and spinal) to treat a traumatic/pathological fracture, to fuse a joint (arthrodesis) and/or as part of an osteotomy. Typically attached to a bone of a limb, rib, sternum, or pelvis, it is designed to be fixed in place with screws, and may be used in connection with another fixation plate; it does not incorporate a sleeve or blade. Disposable instruments intended to facilitate implantation, or fixation implants (i.e., bone screws), may be packaged with the plate.

Regulatory Flags#

DUNS number
480054895
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
true
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
07630894821424APTUSP-4031.01P-4031.012026-10-27
07630894821431APTUSP-4031.02P-4031.022026-10-27
07630894821448APTUSP-4031.03P-4031.032026-10-27
07630894821455APTUSP-4031.04P-4031.042026-10-27
07630894821462APTUSP-4031.05P-4031.052026-10-27
07630894821479APTUSP-4031.06P-4031.062026-10-27
07630894821486APTUSP-4031.07P-4031.072026-10-27
07630894821493APTUSP-4031.08P-4031.082026-10-27
07630894821509APTUSP-4031.09P-4031.092026-10-27
07630894821516APTUSP-4031.10P-4031.102026-10-27
07630894821523APTUSP-4031.21P-4031.212026-10-27
07630894821530APTUSP-4031.22P-4031.222026-10-27
07630894821547APTUSP-4031.23P-4031.232026-10-27
07630894821554APTUSP-4031.24P-4031.242026-10-27
07630894821561APTUSP-4031.30/1P-4031.30/12026-10-27
07630894821578APTUSP-4031.01SP-4031.01S2026-10-27
07630894821585APTUSP-4031.02SP-4031.02S2026-10-27
07630894821592APTUSP-4031.03SP-4031.03S2026-10-27
07630894821608APTUSP-4031.04SP-4031.04S2026-10-27
07630894821615APTUSP-4031.05SP-4031.05S2026-10-27

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Primary DI, Brand, Company table
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