FDA UDI In Commercial Distribution 🇺🇸 United States

MySpine Unilateral Guide

DI: 07630345786227 · Model: 7.1002 · Medacta International SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MySpine Unilateral Guide
Primary DI
07630345786227
Version / Model
7.1002
Company Name
Medacta International SA
Labeler DUNS
488227125
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-25
Public Version
1
Public Version Date
2023-08-02
Public Version Status
New
Public Device Record Key
455ede3a-53a6-4e01-bfde-ee0ba91c97a7

Device Description

MySpine Unilateral left guide T02

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
PQC Pedicle Screw Placement Guide

GMDN Terms

Code Name
58927 Orthopaedic prosthesis implantation positioning instrument, single-use

Identifiers

Type ID
Primary 07630345786227

Premarket Submissions

Submission Number Supplement Number
K231483 000