FDA UDI In Commercial Distribution 🇺🇸 United States

BALLISTA PERCUTANEOUS PEDICLE SCREW SYSTEM

DI: 00888480211501 · Model: 2000-5290 · BIOMET SPINE LLC
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BALLISTA PERCUTANEOUS PEDICLE SCREW SYSTEM
Primary DI
00888480211501
Version / Model
2000-5290
Catalog Number
2000-5290
Company Name
BIOMET SPINE LLC
Labeler DUNS
018577570
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
3
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
9adf684b-dea8-4fea-94a7-e85577c4c2d7

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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MNH Orthosis, spondylolisthesis spinal fixation
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 00888480211501

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 90MM PERCUTANEOUS ROD