(a) Should result in the collection of useful data that will address the postmarket surveillance question |
An approval order, identifying any specific requirements related to your postmarket surveillance |
Conduct postmarket surveillance of your device in accordance with the approved plan |
(b) Should result in the collection of useful data that will address the postmarket surveillance question after specific revisions are made or specific information is provided |
An approvable letter identifying the specific revisions or information that must be submitted before your plan can be approved |
Revise your postmarket surveillance submission to address the concerns in the approvable letter and submit it to us within the specified timeframe. We will determine the timeframe case-by-case, based on the types of revisions or information that you must submit |
(c) Does not meet the requirements specified in this part |
A letter disapproving your plan and identifying the reasons for disapproval |
Revise your postmarket surveillance submission and submit it to us within the specified timeframe. We will determine the timeframe case-by-case, based on the types of revisions or information that you must submit |
(d) Is not likely to result in the collection of useful data that will address the postmarket surveillance question |
A letter disapproving your plan and identifying the reasons for disapproval |
Revise your postmarket surveillance submission and submit it to us within the specified timeframe. We will determine the timeframe case-by-case, based on the types of revisions or information that you must submit |