Atlas FDA

Simplify Disc

FDA 510(k) clearance K211757 · decided 2021-08-20

Clearance details

K-number
K211757
Device name
Simplify Disc
Applicant
Nuvasive, Inc.
Decision
Substantially Equivalent
Date received
2021-06-07
Decision date
2021-08-20
Days to decision
74 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

+ Add to Predicate Builder ◉ Watch Nuvasive

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

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

RecordFirmDate
Synergy Disc Instruments (K253392)Synergy Spine Solutions, Inc.2026-03-27
prodisc® L Instruments (K250554)Centinel Spine, LLC2025-04-25
prodisc® L Instruments (K242869)Centinel Spine, LLC2024-12-17
M6-C™ Single Use, Disposable Instrumentation (K241117)Spinal Kinetics / Orthofix / Seaspine2024-06-21
activL® Next Generation Instrumentation (K231769)Aesculap Implants Systems, LLC2023-07-13
prodisc C SK, prodisc C Nova, and prodisc C Vivo Instruments (K221848)Centinel Spine, LLC2022-08-19
M6-C Artificial Cervical Disc Instruments AS (K220861)Spinal Kinetics, LLC2022-06-02

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
Simplify® Cervical Artificial Disc (P200022/S016)Nuvasive, Inc.2025-06-05
Simplify® Cervical Artificial Disc (P200022/S017)Nuvasive, Inc.2025-05-29
Simplify Disc (P200022/S012)Nuvasive, Inc.2025-02-18
Simplify Cervical Artificial Disc (P200022/S015)Nuvasive, Inc.2025-02-13
Simplify Cervical Artificial Disc (P200022/S014)Nuvasive, Inc.2024-12-18
Simplify® Cervical Artificial Disc (P200022/S013)Nuvasive, Inc.2024-04-17
Simplify Disc (P200022/S011)Nuvasive, Inc.2023-06-09
Simplify Cervical Artificial Disc (P200022/S010)Nuvasive, Inc.2023-03-15