FDA UDI Not in Commercial Distribution 🇺🇸 United States

Matrix

DI: 10705034746326 · Model: 04.633.160 · SYNTHES (U.S.A.) LP
Product Codes
5
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Matrix
Primary DI
10705034746326
Version / Model
04.633.160
Catalog Number
04633160
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
4
Public Version Date
2020-09-17
Public Version Status
Update
Public Device Record Key
74d56416-9c3d-4458-ac2c-e2181d72bef9
Distribution End Date
2020-09-17

Device Description

5.5MM TI MATRIX MONOAXIAL SCREW 60MM THREAD LENGTH

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
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
MNH Orthosis, spondylolisthesis spinal fixation
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Secondary H981046331600
Primary 10705034746326

Customer Contacts