The following data is part of a premarket notification filed by Innovasive Devices, Inc. with the FDA for Innovasive Devices Intratunnel Tibial Fixation Fastener.
Device ID | K983560 |
510k Number | K983560 |
Device Name: | INNOVASIVE DEVICES INTRATUNNEL TIBIAL FIXATION FASTENER |
Classification | Fastener, Fixation, Nondegradable, Soft Tissue |
Applicant | INNOVASIVE DEVICES, INC. 734 FOREST ST. Marlborough, MA 01752 |
Contact | Eric Bannon |
Correspondent | Eric Bannon INNOVASIVE DEVICES, INC. 734 FOREST ST. Marlborough, MA 01752 |
Product Code | MBI |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-10-13 |
Decision Date | 1999-01-28 |
Summary: | summary |