FDA 510(k) Applications Submitted by LI MEDICAL TECHNOLOGIES, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K963812 |
09/09/1996 |
LM BONE ANCHOR (ORTHOPEDICS) |
LI MEDICAL TECHNOLOGIES, INC. |
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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