FDA 510(k) Applications Submitted by RHODEMANN LI
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K960448 |
01/30/1996 |
LM ANCHOR |
LI MEDICAL TECHNOLOGIES, INC. |
| K960439 |
01/31/1996 |
LM BONE ANCHOR |
LI MEDICAL TECHNOLOGIES, INC. |
| K960825 |
02/29/1996 |
LM ANCHOR OR OTHER PROPRIETARY NAME |
LI MEDICAL TECHNOLOGIES, INC. |
| K981755 |
05/18/1998 |
LM ANCHOR |
LI MEDICAL TECHNOLOGIES, INC. |
| K981764 |
05/19/1998 |
LM ANCHOR |
LI MEDICAL TECHNOLOGIES, INC. |
| K002413 |
08/07/2000 |
ULTRASORB SUTURE ANCHOR |
LI MEDICAL TECHNOLOGIES, INC. |
| K963288 |
08/21/1996 |
LM BONE ANCHOR |
LI MEDICAL TECHNOLOGIES, INC. |
| K992938 |
08/31/1999 |
ROTORBLADE SUTURE ANCHOR |
LI MEDICAL TECHNOLOGIES, INC. |
| K983435 |
09/29/1998 |
ROTORBLADE |
LI MEDICAL TECHNOLOGIES, INC. |
| K993373 |
10/07/1999 |
ROTORBLADE SUTURE ANCHOR |
LI MEDICAL TECHNOLOGIES, INC. |
|
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