FDA UDI Not in Commercial Distribution 🇺🇸 United States

PERIMETER Spinal System

DI: 00643169584068 · Model: X1214495 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PERIMETER Spinal System
Primary DI
00643169584068
Version / Model
X1214495
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-17
Public Version
5
Public Version Date
2022-05-09
Public Version Status
Update
Public Device Record Key
d8038d09-a518-418e-a0e5-5a9e54f47142
Distribution End Date
2022-05-04

Device Description

TRIAL X1214495 PER XXL 15DEG 16MM

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
Yes
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
44788 Spinal implant trial

Identifiers

Type ID
Primary 00643169584068

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K160418 000

Device Sizes

Type Value Unit Text
Width 38.0 Millimeter
Height 16.0 Millimeter
Length 28.0 Millimeter
Angle 15.0 degree