FDA UDI In Commercial Distribution 🇺🇸 United States

Sagittae

DI: 00819837021085 · Model: 903-030-XX · SPINEEX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sagittae
Primary DI
00819837021085
Version / Model
903-030-XX
Catalog Number
903-030-XX
Company Name
SPINEEX, INC.
Labeler DUNS
080723590
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-14
Public Version
1
Public Version Date
2020-05-22
Public Version Status
New
Public Device Record Key
b294b843-a385-41c6-8d23-5684b3eb447e

Device Description

MIS Handle

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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
47829 Surgical instrument handle, non-torque-limiting

Identifiers

Type ID
Primary 00819837021085

Customer Contacts

Phone
5135736165

Premarket Submissions

Submission Number Supplement Number
K200816 000