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 |