Device Classification Name |
Holder, Needle; Orthopedic
|
510(k) Number |
K860018 |
Device Name |
FISCHER WIRE/PIN CLAMP |
Applicant |
BUCKMAN CO., INC. |
921 CALLE VERDE |
MARTINEZ,
CA
94553
|
|
Applicant Contact |
DAVID W SCHLERF |
Correspondent |
BUCKMAN CO., INC. |
921 CALLE VERDE |
MARTINEZ,
CA
94553
|
|
Correspondent Contact |
DAVID W SCHLERF |
Regulation Number | 888.4540
|
Classification Product Code |
|
Date Received | 01/03/1986 |
Decision Date | 02/07/1986 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Orthopedic
|
510k Review Panel |
Orthopedic
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|