The following data is part of a premarket notification filed by Synvasive Technology, Inc. with the FDA for Hedleyl Intramedullary Preparation Brush.
Device ID | K931737 |
510k Number | K931737 |
Device Name: | HEDLEYL INTRAMEDULLARY PREPARATION BRUSH |
Classification | Instrument, Cutting, Orthopedic |
Applicant | SYNVASIVE TECHNOLOGY, INC. 11328 SUNRISE GOLD CIRCLE Rancho Cordova, CA 95742 |
Contact | Carol Laufenberg |
Correspondent | Carol Laufenberg SYNVASIVE TECHNOLOGY, INC. 11328 SUNRISE GOLD CIRCLE Rancho Cordova, CA 95742 |
Product Code | HTZ |
CFR Regulation Number | 878.4800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-04-07 |
Decision Date | 1994-01-07 |