Atlas FDA

X STOP INTERSPINOUS PROCESS DECOMPRESSION SYSTEM

FDA premarket approval P040001 · decided 2005-11-21

Approval details

PMA number
P040001
Trade name
X STOP INTERSPINOUS PROCESS DECOMPRESSION SYSTEM
Generic name
Prosthesis, spinous process spacer/plate
Applicant
Medtronic Sofamor Danek, Inc.
Date received
2004-01-06
Decision date
2005-11-21
Days to decision
685 days
Decision code
APWD
Product code
NQO
Advisory committee
Orthopedic
Expedited review
Yes
Location
Memphis, TN
Statement
APPROVAL FOR THE X STOP INTERSPINOUS PROCESS DECOMPRESSION SYSTEM. THE DEVICE IS INDICATED FOR TREATMENT OF PATIENTS AGED 50 OR OLDER SUFFERING FROM NEUROGENIC INTERMITTENT CLAUDICATION SECONDARY TO A CONFIRMED DIAGNOSIS OF LUMBAR SPINAL STENOSIS (WITH X-RAY, MRI, AND /OR CT EVIDENCE OF THICKENED LIGAMENTUM FLAVUM, NARROWED LATERAL RECESS AND/OR CENTRAL CANAL NARROWING). THE X STOP IS INDICATED FOR THOSE PATIENTS WITH MODERATELY IMPAIRED PHYSICAL FUNCTION WHO EXPERIENCE RELIEF IN FLEXION FROM TH

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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