Atlas FDA

CD HORIZON SPINAL SYSTEM

FDA 510(k) clearance K061304 · decided 2006-07-18

Clearance details

K-number
K061304
Device name
CD HORIZON SPINAL SYSTEM
Applicant
Medtronic Sofamor Danek
Decision
Substantially Equivalent
Date received
2006-05-10
Decision date
2006-07-18
Days to decision
69 days
Clearance type
Traditional
Product code
NQP
Device class
2
Regulation number
888.3070
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Memphis, TN, 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
CD HORIZON™ Spinal System (K203678)Medtronic Sofamor Danek USA, Inc.2021-01-15
CD Horizon™ Astute™ Spinal System (K191066)Medtronic Sofamor Danek USA, Inc.2019-10-03
CD Horizon™ Spinal System (K182928)Medtronic Sofamor Danek USA, Inc.2019-01-11
DYNESYS TOP-LOADING SPINAL SYSTEM (K133164)Zimmer Spine, Inc.2014-01-16
ZIMMER DTO PIN PRESS INSTRUMENT (K101704)Zimmer Spine, Inc.2010-08-18
DSS STABILIZATION SYSTEM (K101083)Paradigm Spine, LLC2010-07-02
DYNESYS TOP-LOADING SPINAL SYSTEM (K092234)Zimmer Spine, Inc.2009-10-01
MODIFICATION TO: DSS STABILIZATION SYSTEM (K091944)Paradigm Spine, LLC2009-08-03
TRANSITION STABILIZATION SYSTEM (K073439)Globus Medical, Inc.2009-02-20
DDS STABILIZATION SYSTEM (K080241)Paradigm Spine, LLC2008-11-28
DSS STABILIZATION SYSTEM (K080963)Paradigm Spine2008-05-02
ISOBAR SEMI-RIGID DUAL DAMPENER (K071261)Scient'X2008-04-17

Recalls involving this device

No recalls on record reference this clearance.