American Medical Electronics, Inc. - FDA 510(k) Cleared Devices
14
Total
11
Cleared
0
Denied
American Medical Electronics, Inc. has 11 FDA 510(k) cleared orthopedic devices. Based in Dallas, US.
Historical record: 11 cleared submissions from 1989 to 1995.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Aug 25, 1995
EXPANDED RANGE OF SUTURE SIZES OGDEN ANCHORS: 7.4MM AND 5.5MM
Orthopedic
158d
Cleared
Aug 21, 1995
OGDEN ANCHOR
Orthopedic
94d
Cleared
Jul 11, 1995
OGDEN ANCHOR
Orthopedic
133d
Cleared
Jul 03, 1995
OGDEN ANCHOR
Orthopedic
94d
Cleared
Jul 03, 1995
OGDEN ANCHOR FOR ALL ORTHOPAEDIC SOFT TISSUE APPLICATIONS
Orthopedic
95d
Cleared
Feb 09, 1995
OGDEN ANCHOR-SMALL (TENTATIVE)
Orthopedic
339d
Cleared
Feb 01, 1995
AME UNIVERSAL FIXATION SYSTEM
Orthopedic
685d
Cleared
Jan 30, 1995
OGDEN ANCHOR ADDITIONAL APPLICATIONS
Orthopedic
467d
Cleared
Jan 09, 1995
SILKON TITANIUM CABLE SYSTEM
Orthopedic
242d
Cleared
Jul 12, 1994
OGDEN ANCHOR (MODIFICATION)
Orthopedic
258d
Cleared
May 03, 1994
AME(R) UNIVERSIAL CABLE SYSTEM
Orthopedic
334d
Cleared
Feb 22, 1994
AME UNIVERSAL BONE SCREW
Orthopedic
407d
Cleared
Feb 01, 1994
AME(R) RIGID FIXATION SYSTEM
Orthopedic
364d
Cleared
Feb 10, 1989
AME PINSITE SHIELD(TM)
Orthopedic
86d