FDA UDI In Commercial Distribution 🇺🇸 United States

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DI: M7401610003 · Model: 16-02-01-2 · SPINEOLOGY INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Navigation
Primary DI
M7401610003
Version / Model
16-02-01-2
Catalog Number
161-0003
Company Name
SPINEOLOGY INC.
Labeler DUNS
033014361
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-28
Public Version
1
Public Version Date
2018-09-28
Public Version Status
New
Public Device Record Key
ebe3091b-5b6a-4e82-a148-4bffb3d4d420

Device Description

Cannulated Tap, 5.5

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
MR Unsafe
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
OLO Orthopedic stereotaxic instrument

GMDN Terms

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

Identifiers

Type ID
Primary M7401610003

Customer Contacts

Phone
+1(651)256-8500 ext. 513

Premarket Submissions

Submission Number Supplement Number
K180796 000

Device Sizes

Type Value Unit Text
Outer Diameter 5.5 Millimeter
Device Size Text, specify Cannulated Bone Tap, 5.5mm