The following data is part of a premarket notification filed by Waldemar Link Gmbh & Co. Kg with the FDA for Mobilelink Acetabular Cup System.
Device ID | K182321 |
510k Number | K182321 |
Device Name: | MobileLink Acetabular Cup System |
Classification | Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented |
Applicant | Waldemar Link GmbH & Co. KG Oststrabe 4-10 Norderstedt, DE 22844 |
Contact | Karen Sonnenberger |
Correspondent | Karen Sonnenberger Waldemar Link GmbH & Co. KG Oststrabe 4-10 Norderstedt, DE 22844 |
Product Code | LZO |
Subsequent Product Code | LPH |
Subsequent Product Code | MEH |
Subsequent Product Code | OQG |
CFR Regulation Number | 888.3353 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-08-27 |
Decision Date | 2019-05-24 |