FDA 510(k) Applications Submitted by Lynne Witkowski
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K990030 |
01/05/1999 |
ADVANCED REVISION PRODUCT LINE EXTENSION |
WRIGHT MEDICAL TECHNOLOGY, INC. |
| K980496 |
02/09/1998 |
WRIGHT MEDICAL TECHNOLOGY ROD-TO-ROD COUPLER |
WRIGHT MEDICAL TECHNOLOGY, INC. |
| K991123 |
04/02/1999 |
PERFECTA RS LATERALIZED HIP STEM, BRIDGE HIP SYSTEM |
WRIGHT MEDICAL TECHNOLOGY, INC. |
| K090973 |
04/06/2009 |
TERUMO SURSHIELD SAFETY I.V. CATHETER (18G X 51MM & 20G X 51MM SIZES) |
TERUMO CORP. |
| K001706 |
06/05/2000 |
WMT MODULAR SHOULDER SYSTEM |
WRIGHT MEDICAL TECHNOLOGY, INC. |
| K991915 |
06/07/1999 |
MODULAR RADIAL HEAD |
WRIGHT MEDICAL TECHNOLOGY, INC. |
| K982390 |
07/09/1998 |
CONCISE COMPRESSION HIP SCREW SYSTEM (STERILE) |
WRIGHT MEDICAL TECHNOLOGY, INC. |
| K993371 |
10/07/1999 |
SADDLE SHAPED PATELLA |
WRIGHT MEDICAL TECHNOLOGY, INC. |
| K994061 |
12/01/1999 |
LOCON-T DISTAL RADIAL PLATE |
WRIGHT MEDICAL TECHNOLOGY, INC. |
| K230036 |
12/27/2022 |
Pre-Sutured Tendon (4561SC / Single Strand); Pre-Sutured Tendon (4564SC / Quadruple Strand ) |
RTI Surgical, Inc |
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