Atlas FDA

X-STOP INTERSPINOUS DECOMPRESSION SYSTEM

FDA premarket approval P040001/S005 · decided 2007-11-20

Approval details

PMA number
P040001
Supplement
S005
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol - OSB
Trade name
X-STOP INTERSPINOUS DECOMPRESSION SYSTEM
Generic name
Prosthesis, spinous process spacer/plate
Applicant
Medtronic Sofamor Danek, Inc.
Date received
2007-03-30
Decision date
2007-11-20
Days to decision
235 days
Decision code
APPR
Product code
NQO
Advisory committee
Orthopedic
Expedited review
No
Location
Memphis, TN
Statement
APPROVAL OF THE POST-APPROVAL STUDY.

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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