The following data is part of a premarket notification filed by Stryker Orthopaedics with the FDA for Restoration Anatomic Shell.
Device ID | K151264 |
510k Number | K151264 |
Device Name: | Restoration Anatomic Shell |
Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
Applicant | STRYKER ORTHOPAEDICS 325 Corporate Drive Mahwah, NJ 07430 |
Contact | Allison M Ling |
Correspondent | Allison M Ling STRYKER ORTHOPAEDICS 325 Corporate Drive Mahwah, NJ 07430 |
Product Code | LPH |
CFR Regulation Number | 888.3358 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-05-13 |
Decision Date | 2015-08-10 |
Summary: | summary |