FDA 510(k) Applications Submitted by VERNON C BROWN
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K010124 |
01/16/2001 |
ARTHREX UNIVERS 30 SHOULDER PROSTHESIS |
ARTHREX, INC. |
| K020345 |
02/01/2002 |
ARTHREX UNIVERS FRACTURE PROSTHESIS |
ARTHREX, INC. |
| K000506 |
02/15/2000 |
BIO-FASTAK SUTURE ANCHOR, MODEL AR-1324B |
ARTHREX, INC. |
| K010457 |
02/16/2001 |
ARTHREX TWISTLOC SUTURE ANCHOR, MODEL AR-1924 |
ARTHREX, INC. |
| K010525 |
02/22/2001 |
ARTHREX TENODESIS SCREW 7MM, 8MM, 9MM |
ARTHREX, INC. |
| K990987 |
03/24/1999 |
BIO-ABSORBABLE CORKSCREW, MODEL AR-1920B |
ARTHREX, INC. |
| K011172 |
04/17/2001 |
ARTHREX BIO-TRANSFIX |
ARTHREX, INC. |
| K003227 |
10/16/2000 |
BIO-ABSORBABLE CORKSCREW MODEL AR-1920B |
ARTHREX, INC. |
| K990340 |
02/03/1999 |
ARTHREX PLA TISSUETAK, MODEL # AR-1940 BU |
ARTHREX, INC. |
| K990361 |
02/05/1999 |
HEADED BIO-ABSORBABLE CORKSCREW MODEL #AR-1921BU |
ARTHREX, INC. |
| K991971 |
06/11/1999 |
ARTHREX CHONDRAL DART, MODEL AR-4005B-18 |
ARTHREX, INC. |
| K003816 |
12/11/2000 |
ARTHREX TITANIUM CORKSCREW, 3.5 MM, ARTHREX TITANIUM CORKSCREW, 5.0 MM, ARTHREX TITANIUM CORKSCREW 6.5MM |
ARTHREX, INC. |
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