Atlas FDA

M6-C Artificial Cervical Disc

FDA premarket approval P170036/S014 · decided 2024-06-14

Approval details

PMA number
P170036
Supplement
S014
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
M6-C Artificial Cervical Disc
Generic name
Prosthesis, intervertebral disc
Applicant
Spinal Kinetics, LLC
Date received
2024-05-16
Decision date
2024-06-14
Days to decision
29 days
Decision code
OK30
Product code
MJO
Advisory committee
Orthopedic
Expedited review
No
Location
Sunnyvale, CA
Statement
approval of use of the Keyence Laser Marking System for marking the device endplate

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510(k) clearances by this applicant

RecordFirmDate
M6-C Artificial Cervical Disc Instruments AS (K220861)Spinal Kinetics, LLC2022-06-02