Atlas FDA

X-STOP INTERSPINOUS SPACER SYSTEM

FDA premarket approval P040001/S019 · decided 2011-05-04

Approval details

PMA number
P040001
Supplement
S019
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
X-STOP INTERSPINOUS SPACER SYSTEM
Generic name
Prosthesis, spinous process spacer/plate
Applicant
Medtronic Sofamor Danek, Inc.
Date received
2011-03-08
Decision date
2011-05-04
Days to decision
57 days
Decision code
APPR
Product code
NQO
Advisory committee
Orthopedic
Expedited review
No
Location
Memphis, TN
Statement
APPROVAL FOR IMPLEMENTATION OF NEW INSTRUMENT CLEANING AND STERILIZATION PROCESSES AND 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 SPACER IS INDICATED FOR THOSE PATIENTS WITH MODERATELY IMPAIRED PHYSICAL FUNCTION WHO EXPERIENCE RELIEF IN

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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