The following data is part of a premarket notification filed by Isto Technologies, Inc. with the FDA for Inqu Paste Mix Plus.
Device ID | K103799 |
510k Number | K103799 |
Device Name: | INQU PASTE MIX PLUS |
Classification | Filler, Bone Void, Calcium Compound |
Applicant | ISTO TECHNOLOGIES, INC. 5600 WISCONSIN AVE. #509 Chevy Chase, MD 20815 |
Contact | Patsy J Trisler, Jd, Rac |
Correspondent | Patsy J Trisler, Jd, Rac ISTO TECHNOLOGIES, INC. 5600 WISCONSIN AVE. #509 Chevy Chase, MD 20815 |
Product Code | MQV |
CFR Regulation Number | 888.3045 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-12-28 |
Decision Date | 2011-08-29 |
Summary: | summary |