FDA UDI In Commercial Distribution 🇺🇸 United States

ZIP

DI: B5211040100370 · Model: 51 · AURORA SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ZIP
Primary DI
B5211040100370
Version / Model
51
Catalog Number
104-010-037
Company Name
AURORA SPINE, INC.
Labeler DUNS
079119091
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-01
Public Version
2
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
feb4600f-b7ec-4026-a505-46539f249b11

Device Description

ZIP 51 MIS Interspinous Fusion System, 10mm x 37mm

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
PEK Spinous Process Plate

GMDN Terms

Code Name
61688 Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile

Identifiers

Type ID
Primary B5211040100370

Customer Contacts

Phone
760.424.2004

Premarket Submissions

Submission Number Supplement Number
K141317 000

Device Sizes

Type Value Unit Text
Length 37 Millimeter
Lumen/Inner Diameter 10 Millimeter