The following data is part of a premarket notification filed by Stryker Endoscopy with the FDA for Thermo-plastic Shaver Blades.
Device ID | K963332 |
510k Number | K963332 |
Device Name: | THERMO-PLASTIC SHAVER BLADES |
Classification | Arthroscope |
Applicant | Stryker Endoscopy 2590 WALSH AVE. Santa Clara, CA 95051 -4085 |
Contact | Eric Finley |
Correspondent | Eric Finley Stryker Endoscopy 2590 WALSH AVE. Santa Clara, CA 95051 -4085 |
Product Code | HRX |
CFR Regulation Number | 888.1100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-08-23 |
Decision Date | 1996-10-11 |
Summary: | summary |