Atlas FDA

MODIFICATION TO CD HORIZON SPINAL SYSTEM

FDA 510(k) clearance K000094 · decided 2000-02-08

Clearance details

K-number
K000094
Device name
MODIFICATION TO CD HORIZON SPINAL SYSTEM
Applicant
Medtronic Sofamor Danek USA, Inc.
Decision
Substantially Equivalent
Date received
2000-01-13
Decision date
2000-02-08
Days to decision
26 days
Clearance type
Special
Product code
MNH
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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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
INFUSE® Bone Graft/LT-Cage Lumbar Tapered Fusion Device (P000058/S094)Medtronic Sofamor Danek USA, Inc.2025-03-19
INFUSE® Bone Graft (P000054/S074)Medtronic Sofamor Danek USA, Inc.2025-03-19
INFUSE™ Bone Graft/Medtronic Interbody Fusion Device (P000058/S093)Medtronic Sofamor Danek USA, Inc.2024-11-06
INFUSE™ Bone Graft (P000054/S073)Medtronic Sofamor Danek USA, Inc.2024-11-06
Prestige LP (R) Cervical Disc (P090029/S021)Medtronic Sofamor Danek USA, Inc.2024-08-09
Prestige LP (R) Cervical Disc (P090029/S020)Medtronic Sofamor Danek USA, Inc.2024-05-01
Prestige LP Cervical Disc (P090029/S018)Medtronic Sofamor Danek USA, Inc.2024-02-21
Prestige LP® Cervical Disc (P090029/S019)Medtronic Sofamor Danek USA, Inc.2023-10-26