21 CFR 888.3085 — Intervertebral Body Graft Containment Device
Orthopedic (OR) · Part 888 Subpart D—Prosthetic Devices · § 888.3085
Identification
An intervertebral body graft containment device is a non-rigid, implanted spinal device that is designed to contain bone graft within its internal cavity. The device is inserted into the intervertebral body space of the spine and is intended as an adjunct to intervertebral body fusion.
Classification Rationale
Class II (special controls). The special controls for this device are:
Product Codes
| Product Code | Device Name | Class | Devices | Attributes |
|---|---|---|---|---|
| OQB | Intervertebral Body Graft Containment Device | 2 | 4 | Implant |
Special Controls
OQB — Intervertebral Body Graft Containment Device
*Classification.* Class II (special controls). The special controls for this device are:(1) Clinical performance testing must include an assessment of any adverse events observed during clinical use, as well as intervertebral body fusion, and compare this to a clinically acceptable fusion rate. (2) Non-clinical performance testing must demonstrate the mechanical function and durability of the implant, as well as the ability of the device to be inserted, deployed, and filled with bone graft consistently. (3) Device must be demonstrated to be biocompatible. (4) Validation testing must demonstrate the cleanliness and sterility of, or the ability to clean and sterilize, the device components, and device-specific instruments. (5) Design characteristics of the device, including engineering schematics, must ensure that the geometry and material composition are consistent with the intended use. (6) Labeling must bear all information required for the safe and effective use of the device, specifically including the following: (i) A clear description of the technological features of the device including identification of device materials, compatible components in the fusion construct, and the principles of device operation; (ii) Intended use and indications for use, including levels of fixation; (iii) Identification of magnetic resonance (MR) compatibility status; (iv) Cleaning and sterilization instructions for devices and instruments that are provided nonsterile to the end user; and (v) Detailed instructions of each surgical step, including device removal.
eCFR
OQB — Intervertebral Body Graft Containment Device
(1) Clinical performance testing must include an assessment of any adverse events observed during clinical use, as well as intervertebral body fusion, and compare this to a clinically acceptable fusion rate. (2) Non-clinical performance testing must demonstrate the mechanical function and durability of the implant, as well as the ability of the device to be inserted, deployed, and filled with bone graft consistently. (3) Device must be demonstrated to be biocompatible. (4) Validation testing must demonstrate the cleanliness and sterility of, or the ability to clean and sterilize, the device components, and device-specific instruments. (5) Design characteristics of the device, including engineering schematics, must ensure that the geometry and material composition are consistent with the intended use. (6) Labeling must bear all information required for the safe and effective use of the device, specifically including the following: (i) A clear description of the technological features of the device including identification of device materials, compatible components in the fusion construct, and the principles of device operation; (ii) Intended use and indications for use, including levels of fixation; (iii) Identification of magnetic resonance (MR) compatibility status; (iv) Cleaning and sterilization instructions for devices and instruments that are provided nonsterile to the end user; and (v) Detailed instructions of each surgical step, including device removal.
Ecfr Llm
