FDA UDI In Commercial Distribution 🇺🇸 United States

PathFinder NXT®

DI: 00889024336513 · Model: 3572-1 · BIOMET SPINE LLC
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PathFinder NXT®
Primary DI
00889024336513
Version / Model
3572-1
Catalog Number
3572-1
Company Name
BIOMET SPINE LLC
Labeler DUNS
018577570
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-23
Public Version
4
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
d57fc097-2dc3-422a-85e0-b18f1e27a7b5

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
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease
MNH Orthosis, spondylolisthesis spinal fixation
MNI ORTHOSIS, SPINAL PEDICLE FIXATION

GMDN Terms

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

Identifiers

Type ID
Primary 00889024336513

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Modular T-Handle, 1/4 in (6.35 mm) Square, 3-Position Ratcheting Torque Limiting 90 in-lbs (10.2 N•m)