Atlas FDA

PRESTIGE CERVICAL DISC

FDA premarket approval P060018/S003 · decided 2013-07-12

Approval details

PMA number
P060018
Supplement
S003
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
PRESTIGE CERVICAL DISC
Generic name
Prosthesis, intervertebral disc
Applicant
Medtronic Sofamor Danek, Inc.
Date received
2013-06-14
Decision date
2013-07-12
Days to decision
28 days
Decision code
OK30
Product code
MJO
Advisory committee
Orthopedic
Expedited review
No
Location
Memphis, TN
Statement
CHANGE THE STERILIZATION TESTING PROCEDURE.

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510(k) clearances by this applicant

RecordFirmDate
Grafton™ DBM; Grafton Plus™ DBM Paste; Magnifuse™ Bone Graft (K251193)Medtronic Sofamor Danek, Inc.2025-06-12
Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules (K243706)Medtronic Sofamor Danek, Inc.2025-01-17
Robotic Graft Delivery Instruments (K230716)Medtronic Sofamor Danek, Inc.2023-07-18
MASTERGRAFT MATRIX EXT; MASTERGRAFT PUTTY, MASTERGRAFT STRIP (K141824)Medtronic Sofamor Danek, Inc.2014-09-05
DIVERGENCE MINI-PLATE ANTERIOR CERVICAL FUSION SYSTEM (K140417)Medtronic Sofamor Danek, Inc.2014-07-09
CD HORIZON SPINAL SYSTEM (K140449)Medtronic Sofamor Danek, Inc.2014-03-25
CLYDESDALE SPINAL SYSTEM (K132897)Medtronic Sofamor Danek, Inc.2013-12-11
CRESCENT SPINAL SYSTEM (K133216)Medtronic Sofamor Danek, Inc.2013-11-22