The following data is part of a premarket notification filed by Stryker Endoscopy with the FDA for Stryker Se5 Arthroscopy System With Hermes Voice Control.
Device ID | K974771 |
510k Number | K974771 |
Device Name: | STRYKER SE5 ARTHROSCOPY SYSTEM WITH HERMES VOICE CONTROL |
Classification | Laparoscope, General & Plastic Surgery |
Applicant | Stryker Endoscopy 2590 WALSH AVE. Santa Clara, CA 95051 -4085 |
Contact | Salmaan Hameed |
Correspondent | Salmaan Hameed Stryker Endoscopy 2590 WALSH AVE. Santa Clara, CA 95051 -4085 |
Product Code | GCJ |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-12-22 |
Decision Date | 1998-05-29 |
Summary: | summary |