The following data is part of a premarket notification filed by Walter Lorenz Surgical, Inc. with the FDA for Lorenz Titanium Fracture / Reconstruction Plating System.
Device ID | K001238 |
510k Number | K001238 |
Device Name: | LORENZ TITANIUM FRACTURE / RECONSTRUCTION PLATING SYSTEM |
Classification | Plate, Bone |
Applicant | WALTER LORENZ SURGICAL, INC. 1520 TRADEPORT DR. Jacksonville, FL 32218 |
Contact | Diana Preston |
Correspondent | Diana Preston WALTER LORENZ SURGICAL, INC. 1520 TRADEPORT DR. Jacksonville, FL 32218 |
Product Code | JEY |
CFR Regulation Number | 872.4760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-04-18 |
Decision Date | 2000-05-03 |