Atlas FDA

inVizia Anterior Certical Plate System, SC-AcuFix Ant-Cer Dynamic Cervical Plating System, SC-AcuFix Slimline Anterior Cervical Plate System, SC-AcuFix Thinline Anterior Cervical Plate System, Trinica Anterior Lumbar Plate System, Trinica and Trinica Select Anterior Cervical Plate System, V2F Anterior Fixation System

FDA 510(k) clearance K143626 · decided 2015-03-20

Clearance details

K-number
K143626
Device name
inVizia Anterior Certical Plate System, SC-AcuFix Ant-Cer Dynamic Cervical Plating System, SC-AcuFix Slimline Anterior Cervical Plate System, SC-AcuFix Thinline Anterior Cervical Plate System, Trinica Anterior Lumbar Plate System, Trinica and Trinica Select Anterior Cervical Plate System, V2F Anterior Fixation System
Applicant
Zimmer Spine, Inc.
Decision
Substantially Equivalent
Date received
2014-12-22
Decision date
2015-03-20
Days to decision
88 days
Clearance type
Traditional
Product code
KWQ
Device class
2
Regulation number
888.3060
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Minneapolis, MN, 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.

RecordFirmDate
Palisades™ Buttress Plate System (K261309)Bethesda Medical Devices, LLC2026-07-16
ARIES Anterior Cervical Plate Systems (K252776)ZheJiang Decans Medical Devices Co., Ltd.2026-05-14
CastleLoc-P Anterior Cervical Plate System (K261112)L&K BIOMED Co., Ltd.2026-05-06
corra™ cervical plating system (K260570)Carlsmed, Inc.2026-04-22
VyPlate™ Anterior Cervical Plate System (K260697)Vy Spine, LLC2026-03-27
ANTERIS Thoracolumbar Plate System (K260015)SpineCraft2026-03-04
PathLoc Lumbar Plate System (K251940)L&K BIOMED Co., Ltd.2026-03-03
Aster (K254182)Osteonic Co., Ltd.2026-02-26
Lumbar Spine Truss System - Plating Solution (LSTS-PS) (K253201)4Web, Inc.2026-02-12
aprevo® cervical plating system (K252611)Carlsmed, Inc.2025-12-22
Proximity Anterior Cervical Plate System; Segmental Plating System (SPS) (K251965)Alphatec Spine, Inc.2025-08-28
Resolve Anterior Cervical Plate System (K251436)Pioneer Surgical Technology, Inc.2025-07-11

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
BAK VISTA INTERBODY FUSION CAGE (P950002/S014)Zimmer Spine, Inc.2004-07-01
VISTA LORDOTIC INTERBODY FUSION CAGE (P950002/S013)Zimmer Spine, Inc.2004-01-29
BAK VISTA INTERBODY FUSION CAGE (P950002/S012)Zimmer Spine, Inc.2003-10-31
BAK VISTA INTERBODY FUSION DEVICE (P950002/S011)Zimmer Spine, Inc.2003-07-08
BAK INTERBODY FUSION SYSTEM, BP/LORDOTIC DEVICE (P950002/S007)Zimmer Spine, Inc.2002-05-01
BAK/PROXIMITY(TM) INTERBODY FUSION SYSTEM (P950002/S009)Zimmer Spine, Inc.2001-04-03
BAK/L INTERBODY FUSION SYSTEM (P950002/S008)Zimmer Spine, Inc.1999-12-20
BAK INTERBODY FUSION SYSTEM (P950002/S006)Zimmer Spine, Inc.1998-05-12