FDA UDI In Commercial Distribution 🇺🇸 United States

ZAVATION NanoPrime LABYRINTH PLIF

DI: 00197157069322 · Model: 954-103200-15 · Zavation LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ZAVATION NanoPrime LABYRINTH PLIF
Primary DI
00197157069322
Version / Model
954-103200-15
Company Name
Zavation LLC
Labeler DUNS
069472800
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-06
Public Version
3
Public Version Date
2025-11-20
Public Version Status
Update
Public Device Record Key
18ffcc47-8355-48ea-92b0-0e31579ea249

Device Description

NanoPrime LABYRINTH PLIF 10mmx32mmx0deg -15mm

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
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 00197157069322

Customer Contacts

Phone
6019191119

Premarket Submissions

Submission Number Supplement Number
K233509 000