The following data is part of a premarket notification filed by Coltene/whaledent Inc. with the FDA for Modification Of Parapost Cement.
Device ID | K993710 |
510k Number | K993710 |
Device Name: | MODIFICATION OF PARAPOST CEMENT |
Classification | Cement, Dental |
Applicant | COLTENE/WHALEDENT INC. 750 CORPORATE DR. Mahwah, NJ 07430 -2009 |
Contact | H.j. Vogelstein |
Correspondent | H.j. Vogelstein COLTENE/WHALEDENT INC. 750 CORPORATE DR. Mahwah, NJ 07430 -2009 |
Product Code | EMA |
CFR Regulation Number | 872.3275 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-11-03 |
Decision Date | 1999-12-21 |