Device Classification Name |
fastener, fixation, biodegradable, soft tissue
|
510(k) Number |
K171592 |
Device Name |
CrossFT™ Knotless Biocomposite Suture Anchor with Disposable Driver |
Applicant |
ConMed Corporation |
525 French Road |
Utica,
NY
13502
|
|
Applicant Contact |
Diana L. Nader-Martone |
Correspondent |
ConMed Corporation |
525 French Road |
Utica,
NY
13502
|
|
Correspondent Contact |
Diana L. Nader-Martone |
Regulation Number | 888.3030
|
Classification Product Code |
|
Date Received | 05/31/2017 |
Decision Date | 08/29/2017 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Orthopedic
|
510k Review Panel |
Orthopedic
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|