The following data is part of a premarket notification filed by Howmedica Leibinger, Inc. with the FDA for Leibinger - Luhr Small Mandibular Bone Screws.
Device ID | K963740 |
510k Number | K963740 |
Device Name: | LEIBINGER - LUHR SMALL MANDIBULAR BONE SCREWS |
Classification | Plate, Bone |
Applicant | HOWMEDICA LEIBINGER, INC. 14540 BELTWOOD PARKWAY EAST Dallas, TX 75244 |
Contact | Andrew B Rogers |
Correspondent | Andrew B Rogers HOWMEDICA LEIBINGER, INC. 14540 BELTWOOD PARKWAY EAST Dallas, TX 75244 |
Product Code | JEY |
CFR Regulation Number | 872.4760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-09-17 |
Decision Date | 1996-10-28 |