FDA UDI In Commercial Distribution 🇺🇸 United States

TPLIF Interbody

DI: 00195860009451 · Model: TMP0014 · Evolution Spine LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TPLIF Interbody
Primary DI
00195860009451
Version / Model
TMP0014
Catalog Number
TMP0014
Company Name
Evolution Spine LLC
Labeler DUNS
116940934
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-12
Public Version
1
Public Version Date
2021-06-21
Public Version Status
New
Public Device Record Key
fe5e25fe-8400-4a39-83d8-86d484d418b1

Device Description

11x27x14mm Parallel TPLIF

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
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary 00195860009451

Customer Contacts

Device Sizes

Type Value Unit Text
Depth 27 Millimeter
Height 14 Millimeter
Width 11 Millimeter
Device Size Text, specify Parallel