FDA UDI In Commercial Distribution 🇺🇸 United States

Preference 2

DI: M555286501040 · Model: C · AMEDICA CORPORATION
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Preference 2
Primary DI
M555286501040
Version / Model
C
Catalog Number
28-6501-040
Company Name
AMEDICA CORPORATION
Labeler DUNS
028629553
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-29
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
95365811-2e36-4f16-b146-da771f2fc287

Device Description

ø6.5 x 40mm Reduction Polyaxial Screw Assembly

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
KWQ Appliance, Fixation, Spinal Intervertebral Body
KWP Appliance, Fixation, Spinal Interlaminal
MNI Orthosis, Spinal Pedicle Fixation

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary M555286501040

Customer Contacts

Phone
801-839-3500

Premarket Submissions

Submission Number Supplement Number
K081883 000

Device Sizes

Type Value Unit Text
Outer Diameter 6.5 Millimeter
Length 40 Millimeter