FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10705034787763 · Model: 497.172A · SYNTHES (U.S.A.) LP
Product Codes
5
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10705034787763
Version / Model
497.172A
Catalog Number
497172A
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
2019-06-21
Public Version Status
Update
Public Device Record Key
dd38f99a-1e3c-43e6-8beb-daa0940c4312
Distribution End Date
2019-06-21

Device Description

7.0MM TI VARIABLE AXIS SCREW ASSEMBLY/35MM

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

GMDN Terms

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

Identifiers

Type ID
Secondary H981497172A0
Primary 10705034787763

Customer Contacts