Device Classification Name |
prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
|
510(k) Number |
K211567 |
Device Name |
BiMobile Instruments (for BiMobile Dual Mobility System) |
Applicant |
Waldemar Link GmbH & Co. KG |
Oststraße 4-10 |
Norderstedt,
DE
22844
|
|
Applicant Contact |
Stefanie Fuchs |
Correspondent |
LinkBio Corp. |
Oststraße 4-10 |
Nordertedt,
DE
22844
|
|
Correspondent Contact |
Stefani Fuchs |
Regulation Number | 888.3353
|
Classification Product Code |
|
Subsequent Product Code |
|
Date Received | 05/21/2021 |
Decision Date | 06/03/2022 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Orthopedic
|
510k Review Panel |
Orthopedic
|
Summary |
Summary
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|