FDA UDI In Commercial Distribution 🇺🇸 United States

M6-C

DI: 00812388032609 · Model: 1503-4100.90 · Spinal Kinetics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
M6-C
Primary DI
00812388032609
Version / Model
1503-4100.90
Catalog Number
CIK-300-08
Company Name
Spinal Kinetics, Inc.
Labeler DUNS
171513125
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-09-09
Public Version
1
Public Version Date
2024-09-17
Public Version Status
New
Public Device Record Key
53cb89fe-013d-4230-bc4d-63d7836885aa

Device Description

M6-C Single Use, Disposable Instrumentation: Mallet

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
QLQ Manual Instruments Designed For Use With Total Disc Replacement Devices

GMDN Terms

Code Name
44052 Orthopaedic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 00812388032609

Premarket Submissions

Submission Number Supplement Number
K241117 000