NextAR Spine Platform

Primary DI
07630345709851
Brand
NextAR Spine Platform
Company
Medacta International SA
Model
03.57.10.0061
Device description
NextAR Spine Solid Drill Ø3,6mm depth 20mm
Published
2021-12-07
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Product Codes#

Code, Name table
CodeName
SBFOrthopedic Augmented Reality

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
SBFOrthopedic Augmented RealityNeurology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K210859000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K210859000NextAR™ Spine PlatformMedacta International S.A.2021-11-05SBF

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
07630345709851PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
07630345709851076303457098517630345709851

GMDN Terms#

Term, Definition table
TermDefinition
Optical surgical navigation/tracking systemA mobile assembly of electrically-powered devices intended to provide a physician with optical tools to track manual surgical instruments and locate anatomical structures; it may be intended to overlay pre-acquired radiological images or real-time data [e.g., ultrasound (US)] for surgical navigation, and be capable of creating digital 3-D patient models. It consists of a workstation with controls/display, position/movement tracking cameras (e.g., infrared), adaptors, and sensors/spatial markers designed to be attached to the patient and instruments. It is used for multiple surgical procedures (e.g., craniotomy, tumour resection) in various fields [e.g., ENT, neurosurgery, CMF surgery].

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
488227125
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
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
07630542762482GMK Extension02.12.0110APFL2026-09-18
07630542762499GMK Extension02.12.0110APFR2026-09-18
07630542762505GMK Extension02.12.0111APFL2026-09-18
07630542762512GMK Extension02.12.0111APFR2026-09-18
07630542762529GMK Extension02.12.0112APFL2026-09-18
07630542762536GMK Extension02.12.0112APFR2026-09-18
07630542762543GMK Extension02.12.0113APFL2026-09-18
07630542762550GMK Extension02.12.0113APFR2026-09-18
07630542762567GMK Extension02.12.0114APFL2026-09-18
07630542762574GMK Extension02.12.0114APFR2026-09-18
07630542762581GMK Extension02.12.0117APFL2026-09-18
07630542762598GMK Extension02.12.0117APFR2026-09-18
07630542762604GMK Extension02.12.0120APFL2026-09-18
07630542762611GMK Extension02.12.0120APFR2026-09-18
07630542762628GMK Extension02.12.0210APFL2026-09-18
07630542762635GMK Extension02.12.0210APFR2026-09-18
07630542762642GMK Extension02.12.0211APFL2026-09-18
07630542762659GMK Extension02.12.0211APFR2026-09-18
07630542762666GMK Extension02.12.0212APFL2026-09-18
07630542762673GMK Extension02.12.0212APFR2026-09-18

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Primary DI, Brand, Company table
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07630542720390NextAR Spine PlatformMedacta International SASBF2025-09-19
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