The following data is part of a premarket notification filed by Stryker Instruments with the FDA for Newgen/universal Mandibular System.
Device ID | K014263 |
510k Number | K014263 |
Device Name: | NEWGEN/UNIVERSAL MANDIBULAR SYSTEM |
Classification | Plate, Bone |
Applicant | STRYKER INSTRUMENTS 4100 EAST MILHAM AVE. Kalamazoo, MI 49001 -6197 |
Contact | Robin L Rowe |
Correspondent | Robin L Rowe STRYKER INSTRUMENTS 4100 EAST MILHAM AVE. Kalamazoo, MI 49001 -6197 |
Product Code | JEY |
CFR Regulation Number | 872.4760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-12-27 |
Decision Date | 2002-03-08 |
Summary: | summary |