FDA UDI In Commercial Distribution 🇺🇸 United States

Spinal Instrument

DI: 03700780611348 · Model: 99741001 · CLARIANCE
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Spinal Instrument
Primary DI
03700780611348
Version / Model
99741001
Catalog Number
99741001
Company Name
CLARIANCE
Labeler DUNS
296568400
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-22
Public Version
2
Public Version Date
2018-07-06
Public Version Status
New
Public Device Record Key
3749843e-431d-458a-ad15-edbb8379af28

Device Description

Distractor

Device Characteristics

Single Use
No
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
Yes
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
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation
NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease

GMDN Terms

Code Name
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 03700780611348

Customer Contacts

Phone
7738687041

Premarket Submissions

Submission Number Supplement Number
K120469 000