The following data is part of a premarket notification filed by Stryker Gmbh with the FDA for Asnis® Iii Cannulated Screw System And Asnis® Pro Cannulated Screw System.
Device ID | K213199 |
510k Number | K213199 |
Device Name: | Asnis® III Cannulated Screw System And Asnis® PRO Cannulated Screw System |
Classification | Screw, Fixation, Bone |
Applicant | Stryker GmbH 325 Corporate Drive Mahwah, NJ 07430 |
Contact | Danielle Jannuzzi Madureira |
Correspondent | Danielle Jannuzzi Madureira Stryker GmbH 325 Corporate Drive Mahwah, NJ 07430 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2021-09-29 |
Decision Date | 2022-01-11 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ASNIS 77812391 3802297 Live/Registered |
HOWMEDICA OSTEONICS CORP. 2009-08-25 |
ASNIS 74425232 not registered Dead/Abandoned |
Howmedica Inc. 1993-08-16 |