MySpine Unilateral Guide

Primary DI
07630345786708
Brand
MySpine Unilateral Guide
Company
Medacta International SA
Model
7.1035
Device description
MySpine Unilateral right guide T05
Published
2023-07-25
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
true

Related Records

Product Codes

CodeName
PQCPedicle Screw Placement Guide

Product Code Classifications

CodeDeviceSpecialtyClass
PQCPedicle Screw Placement GuideOrthopedic2

Premarket Submissions

SubmissionSupplement
K231483000

Premarket Details

SubmissionSupplementDeviceApplicantDecision dateProduct code
K231483000MySpine Unilateral GuidesMedacta International S.A.2023-07-21PQC

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
07630345786708PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedEAN-13
07630345786708076303457867087630345786708

GMDN Terms

TermDefinition
Orthopaedic prosthesis implantation positioning instrument, single-useA hand-held surgical instrument intended to be used during implantation of an orthopaedic prosthesis, either manually or as a computer-assisted surgery (CAS) device, to aid in the navigation/placement of the prosthesis or other instruments [e.g., drill sleeves and guide wires (Kirschner wires), patella saw guide]. It may be used for the following applications: 1) to hold/align/fix/guide other instruments, prosthesis, or prosthesis component; 2) to provide relative position landmarks; 3) to ascertain correct spatial orientation or limb alignment; and/or 4) as an interface (non-adaptive) between prosthesis components. This is a single-use device.

Sterilization Methods

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

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07630542790805Mfinity Femoral System01.24.10.3012026-02-27
07630542790812Mfinity Femoral System01.24.10.3022026-02-27
07630542790829Mfinity Femoral System01.24.10.3032026-02-27

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