BONE BAND
Dec 1998
45d
Chapel and Assoc.
1
Total
1
Cleared
0
Denied
Chapel and Assoc. — FDA 510(k) Submissions
Chapel and Assoc. has submitted 1 FDA 510(k) premarket notifications since 1998, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Fixation Accessory . Use the specialty filter in the sidebar to narrow results.
1 devices