R. Thomas Grotz, M.D., Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
R. Thomas Grotz, M.D., Inc. has 4 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Historical record: 4 cleared submissions from 1997 to 1999. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by R. Thomas Grotz, M.D., Inc. Filter by specialty or product code using the sidebar.
4 devices
Cleared
Jan 21, 1999
STABILIZER SOFT TISSUE ANCHOR, 5 AND 8MM
Orthopedic
58d
Cleared
Nov 03, 1997
STABILIZER SOFT TISSUE ANCHOR 5MM MODEL TA1005, ANCHOR INSERTER/SUTURE...
Physical Medicine
81d
Cleared
Feb 18, 1997
STABILIZER SOFT TISSUE ANCHOR MODEL NUMBER TA1005, TA1008, ANCHOR...
Orthopedic
60d
Cleared
Feb 07, 1997
STABILIZER SOFT TISSUE ANCHOR, 8MM MODEL TA1008, ANCHOR INSERTER/SUTURE...
Orthopedic
60d