The following data is part of a premarket notification filed by Waldemar Link Gmbh & Co. Kg with the FDA for Link® Sp-cl® Hip System Porolink® (microporous) And Hx® (cap) Coated & Link® Lcu® Hip System Porolink® (microporous) And Hx® (cap) Coated.
Device ID | K161840 |
510k Number | K161840 |
Device Name: | LINK® SP-CL® Hip System PoroLink® (microporous) And HX® (CaP) Coated & LINK® LCU® Hip System PoroLink® (microporous) And HX® (CaP) Coated |
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 | Lorenz Runge |
Correspondent | Andre Von Malotki Waldemar Link GmbH & Co. KG Oststrabe 4-10 Norderstedt, DE 22844 |
Product Code | LZO |
CFR Regulation Number | 888.3353 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-07-05 |
Decision Date | 2017-03-16 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
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LINK S.R.L. 2022-12-06 |