Atlas FDA

M6-C Artificial Cervical Disc Instruments AS

FDA 510(k) clearance K220861 · decided 2022-06-02

Clearance details

K-number
K220861
Device name
M6-C Artificial Cervical Disc Instruments AS
Applicant
Spinal Kinetics, LLC
Decision
Substantially Equivalent
Date received
2022-03-24
Decision date
2022-06-02
Days to decision
70 days
Clearance type
Traditional
Product code
QLQ
Device class
2
Regulation number
888.4515
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Sunnyvale, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

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Synergy Disc Instruments (K253392)Synergy Spine Solutions, Inc.2026-03-27
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Simplify Disc (K211757)Nuvasive, Inc.2021-08-20

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
M6-C Artificial Cervical Disc (P170036/S016)Spinal Kinetics, LLC2024-08-19
M6-C Artificial Cervical Disc (P170036/S015)Spinal Kinetics, LLC2024-07-10
M6-C Artificial Cervical Disc (P170036/S014)Spinal Kinetics, LLC2024-06-14
M6-C Artificial Cervical Disc (P170036/S013)Spinal Kinetics, LLC2023-06-14
M6-C Artificial Cervical Disc (P170036/S012)Spinal Kinetics, LLC2022-11-01
M6-C Artificial Cervical Disc (P170036/S011)Spinal Kinetics, LLC2022-07-01
M6-C Artificial Cervical Disc (P170036/S010)Spinal Kinetics, LLC2022-04-05
M6-C Artificial Cervial Disc (P170036/S009)Spinal Kinetics, LLC2021-10-12