Atlas FDA

NUVASIVE SPINAL SYSTEM

FDA 510(k) clearance K033546 · decided 2004-04-12

Clearance details

K-number
K033546
Device name
NUVASIVE SPINAL SYSTEM
Applicant
Nuvasive, Inc.
Decision
Substantially Equivalent
Date received
2003-11-12
Decision date
2004-04-12
Days to decision
152 days
Clearance type
Traditional
Product code
MNH
Device class
2
Regulation number
888.3070
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
San Diego, CA, US
Third-party review
No
Expedited review
No

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Captiva Spine and CapLOX II/TowerLOX Pedicle Screw System (K160020)Captiva Spine2016-03-02
Spinal Inner Fixation System (K143013)Changzhou Dingjian Medical Appliance Co., Ltd.2015-12-11
Romeo posterior osteosynthesis system (K151695)Spineart2015-09-10
CapLOX II/TowerLOX Pedicle Screw System (K151116)Captiva Spine2015-06-26
Republic Spine Dark Star Spinal System (K150283)Republic Spine, LLC2015-04-29

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