FDA UDI In Commercial Distribution 🇺🇸 United States

General Instruments

DI: 00840180503591 · Model: CI-10116-10M · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
General Instruments
Primary DI
00840180503591
Version / Model
CI-10116-10M
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-08-06
Public Version
1
Public Version Date
2021-08-16
Public Version Status
New
Public Device Record Key
e0068bac-3a2e-4453-9616-4d2859fd5de6

Device Description

10x12x14mm, 5-deg Pegasus Trials w/Thru Hole

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
OVE Intervertebral fusion device with integrated fixation, cervical

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 00840180503591

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K150913 000

Device Sizes

Type Value Unit Text
Height 10 Millimeter
Width 14 Millimeter
Length 16 Millimeter
Angle 5 degree