Depuy Ace Medical Co. is one of 9126 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Depuy Ace Medical Co. - FDA 510(k) Cleared Devices
Recent clearances: DEPUY ACE SPIDER PLATE, MODIFICATION OF DEPUY ACE TIMAX MEDIAL PILON PLATE, DEPUY ACE SPIDER PLATE
10
Total
10
Cleared
0
Denied
Depuy Ace Medical Co. has 10 FDA 510(k) cleared orthopedic devices. Based in El Segundo, US.
Historical record: 10 cleared submissions from 1997 to 1999.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Depuy Ace Medical Co.
10 devices
Cleared
Mar 23, 1999
DEPUY ACE SPIDER PLATE
Orthopedic
42d
Cleared
Feb 01, 1999
MODIFICATION OF DEPUY ACE TIMAX MEDIAL PILON PLATE
Orthopedic
19d
Cleared
Dec 31, 1998
DEPUY ACE SPIDER PLATE
Orthopedic
16d
Cleared
Dec 22, 1998
DEPUY ACE TIMAX META PLATE
Orthopedic
53d
Cleared
Oct 26, 1998
DEPUY ACE COMPOSITE LOCKING NUT
Orthopedic
39d
Cleared
Aug 31, 1998
DEPUY ACE TIMAX PILON PLATE
Orthopedic
56d
Cleared
Jul 29, 1998
DEPUY ACE TIMAX CALCANEAL PERI-ARTICULAR PLATE
Orthopedic
70d
Cleared
May 22, 1998
DEPUY ACE RING SKULL PINS-MRI, DEPUY ACE SPRING LOADED TONG PIN-MRI, DEPUY...
Orthopedic
191d
Cleared
Apr 30, 1997
DEPUY ACE TROCHANTERIC SIDE PLATE
Orthopedic
79d
Cleared
Mar 21, 1997
DEPUY ACE AIM TITANIUM TIBIAL NAIL
Orthopedic
59d