Failed Medical Device: Blackstone Medical, Inc. ICON Modular Spinal Fixation.
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Transcript of Failed Medical Device: Blackstone Medical, Inc. ICON Modular Spinal Fixation.
Failed Medical Device:Blackstone Medical, Inc. ICON
Modular Spinal Fixation
Brief History• Spinal Fusion – 1950’s• Stress factors directed to
this instrumentation by the human body turned out to be much greater than anticipated leading to a quest for structurally stronger instrumentation
• 1959 – First Screws• 1970’s – First Screws and
Rods• 1983 – First Patent of
this System
Brief History Continued
System Challenges• Nerve Compression• Snapped Screws and
Pedicles • Too Rigid/Too Flexible• Bone Grafting Issues• Muscle Damage
Blackstone Medical, Inc.Products & Services
• Cervical Plate• Laparoscopic Discectomy System• Micro-discectomy System• Discectomy• Blackstone Medical• Blackstone• Blackstone Medical Inc.• Surgical Instruments• Discitis• Spinal Companies• Cervical Spine• Thoracic Spine• Lumbar Spine• Spinal Cord• Herniated Disc• Degenerative Disc• Stenosis• Disc Surgery• Lumbar Discectomy• Desiccated Discs• Removing A Disc• Disk Removal Instruments
Year Established 1996
• Bone Screws
• Spine Surgery• Cage• Medical Devices• Spinal Fusion• Interbody Fusion• Lumbar Spines• Degenerative Disc• Disease• Spinal• Interbody• Implants• Bone• Graft• Lumbar• Spine• Orthopedic Surgery• Back• Back Pain• Lower Back Pain• Low Back Pain• Degenerative Disc Disease• Bone Graft• Titanium Implants
Annual Sales US$10 Million - US$50 Million
Blackstone Medical, Inc.
• Screw and Rod Fixation
• Immobilize and Stabilize Spine Segments at Site of Surgery
ICON Modular Spinal Fixation“A surgical screw system for use with implantation rods includes a screw member, a receiver member, a pressure cap and a locking device. The screw member has a shaft and a head with a spherical undersurface and a conical tapered recess. The receiver member has an upper and lower portion, a u-shaped rod receiving channel and an axial bore. The u-shaped channel has two lateral legs at the upper portion and forms an opening leading to the axial bore. The axial bore near the lower portion includes an inwardly conical tapered surface which has a diameter larger than the shaft of the screw member but smaller than the head of the screw member. The conical surface forms a support upon which the spherical undersurface of the head of the screw member rests when the screw member is guided through the bore of the lower portion of the receiver member. The pressure cap is positioned within the axial bore and situated upon the head of the screw member. The locking device is designed for securing the rod within the u-shaped channel of the receiver member by applying a tightening torque upon the rod when positioned within the opening and the bore near the upper portion of the receiver member.”
Device Components
• Multi Shaft Screw• Fixed Shaft Screw• Bar • Crosslinks• Titanium Alloy
PRODUCT RECALLED!
“The pedicle (vertebra stem) screws may separate from the screw heads, or from the rods that run between
spinal segments. If this happens soon after the surgery, the spine may not fuse properly, and patients may need additional surgery to correct
the problem. If not corrected, some patients may experience long-term
pain and disability. The potential for injury depends on the specific
condition being treated, and the degree of postoperative healing.”
Product availability
• ICON Modular Spinal Fixation System is no longer in use. Similar products are used by other companies.
Replacement or improvement?
• It seems to have been replaced by the SFS or Spinal Fixation System – reduces the need for rod bending – screws can bend with 42° range of motion. – specialized thread minimizes the cross-threading
of the screw
Improvements by the SFS
• 42° range of mobility
• Tapered head for a secure fit
• Threads are triangular in shape
Technological challenges
• Material rejection• Staying in the bone• Staying connected to the supporting rods
Company product testing
• Tension test on screw• Testing of screw rod connection in multiple
environments – Dry– Humid– Wet– Damp
Governmental regulations
• US Food and Drug Administration• Maintain risk analysis of your device in the
design validation• Constant validation of company
documentation and testing
Manufacturing issues
• establish and maintain Corrective and Preventive Action (CAPA) – procedures designed to monitor the cause of the
problems caused by the product
Safety issues
• Class I recall means that death or disability is a possibility– Most serious of recalls issued by FDA
• Additional surgery possibility
Cost effective?
• Less material• Product is useable
Reliability
• Use in lower thoracic and lumber region
Liability
• December 25, 2005 – Blackstone Medical, Inc. informed the FDA of their intention
to recall their product– Notice to surgeons and distributors of the product warning
them of the problem.– Out of 484 surgeries, 4% were returned to surgery for the
removal of the implant.• April 7, 2006
– FDA issued a Class I recall of the ICON Modular Spinal Fixation System.
• Consult with a lawyer if you had spinal surgery in 2005
There’s more. . .• September 2006– Whistleblower lawsuit was filed from an employee,
Susan Hutcheson– Accused Blackstone Medical of giving kickbacks to
surgeons and hospitals who used their implants– Accused Blackstone Medical submitted false claims
to Medicare and Medicaid– Arkansas neurosurgeon, Patrick Chan, has admitted
to receiving kickbacks– Case is still on-going
Developments within the Field
:–Laparoscopic Surgery–BMP – Bone Morphogenetic Protein–Bioabsorbable Implants–Polymers Mimic Characteristics of Bone