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 |