FDA UDI In Commercial Distribution 🇺🇸 United States

SpineNet SSP®

DI: B04710603180 · Model: SSP® Drill Sleeve, 18mm · SPINENET, LLC
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SpineNet SSP®
Primary DI
B04710603180
Version / Model
SSP® Drill Sleeve, 18mm
Catalog Number
106-03-18
Company Name
SPINENET, LLC
Labeler DUNS
792052321
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-13
Public Version
1
Public Version Date
2021-12-22
Public Version Status
New
Public Device Record Key
551a1465-4e06-43f5-ab00-4d97bc382e67

Device Description

SpineNet SSP®, 18mm, Drill Sleeve-Instrument

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
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary B04710603180

Customer Contacts

Phone
407-539-2483

Premarket Submissions

Submission Number Supplement Number
K200170 000