Last synced on 25 April 2025 at 11:05 pm

Osseoanchored Prostheses For The Rehabilitation Of Transfemoral Amputees

Page Type
Product Code
Definition
The device is a percutaneous prosthetic device for the direct skeletal attachment of a prosthetic limb.
Physical State
The device may be threaded, or coated to provide fixation to the bone. The device is made from medical grade metallic components.
Technical Method
The device is implanted into the femur to allow a fixation point for standard prosthetic limbs.
Target Area
Femur of amputee patients.
Review Panel
Orthopedic
Submission Type
PMA
Device Classification
Class 3
GMP Exempt?
No
Summary Malfunction Reporting
Eligible
Implanted Device
Yes
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

The FDA has not linked product code PJY to any particular section of the CFR (Code of Federal Regulations). There are multiple reasons why this might be the case:

  • The product code was created for a class III submission that does not follow the normal PMN or PMA path - e.g., for a device that falls under HDE (Humanitarian Device Exemption) or EUA (Emergency Use Authorization).
  • The FDA has generated the product code for an existing Class III device, as a result of a PMA supplement that modifies the device in a way that it can't fit under the existing product code originally assigned
  • The product code was created for internal use at the FDA, and not for classification or regulatory-related purposes.

Osseoanchored Prostheses For The Rehabilitation Of Transfemoral Amputees

Page Type
Product Code
Definition
The device is a percutaneous prosthetic device for the direct skeletal attachment of a prosthetic limb.
Physical State
The device may be threaded, or coated to provide fixation to the bone. The device is made from medical grade metallic components.
Technical Method
The device is implanted into the femur to allow a fixation point for standard prosthetic limbs.
Target Area
Femur of amputee patients.
Review Panel
Orthopedic
Submission Type
PMA
Device Classification
Class 3
GMP Exempt?
No
Summary Malfunction Reporting
Eligible
Implanted Device
Yes
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

The FDA has not linked product code PJY to any particular section of the CFR (Code of Federal Regulations). There are multiple reasons why this might be the case:

  • The product code was created for a class III submission that does not follow the normal PMN or PMA path - e.g., for a device that falls under HDE (Humanitarian Device Exemption) or EUA (Emergency Use Authorization).
  • The FDA has generated the product code for an existing Class III device, as a result of a PMA supplement that modifies the device in a way that it can't fit under the existing product code originally assigned
  • The product code was created for internal use at the FDA, and not for classification or regulatory-related purposes.