American Orthopaedic Cast Cutter Model 0295-202
Martin Medical
FDA Clearance Information
The American Orthopaedic Cast Cutter Model 0295-202 was cleared through the FDA 510k pathway on March 28, 1986. Manufactured by Martin Medical, it is classified as a Class 1 device under product code LGF.
What It Is
FDA-Cleared Indications
- Removal of orthopedic casts.
Clinical Applications
- Removing casts used to immobilize a healing fracture.
- Removing casts used after orthopedic treatment or intervention.
- Removing rigid orthopedic casts in adult patients.
- Removing rigid orthopedic casts in pediatric patients.
Practical Considerations
- The oscillating blade is designed to cut cast material while reducing the likelihood of cutting the underlying skin, but careful technique is still required.
- Confirm that the blade and device are compatible with the type and thickness of cast material being removed.
- Use by trained orthopedic clinicians, nurses, or cast technicians in an appropriate clinical setting.
- Follow the manufacturer’s instructions for cleaning, maintenance, blade replacement, and infection-control practices.
- This is a mechanical saw, not an MRI-compatible imaging device; keep it outside the MRI scanner room unless the manufacturer has specifically documented its MR safety status.
Frequently Asked Questions
What is the American Orthopaedic Cast Cutter Model 0295-202 used for?
The device is used for safely removing orthopedic casts from patients after the healing process is complete.
What specialties typically use this device?
Orthopedic surgeons, nurses, and cast technicians in orthopedic clinics and hospitals typically use this device.
What are the FDA-cleared indications?
The device is indicated for the removal of orthopedic casts in patients who have been immobilized for fracture healing or other orthopedic conditions.