The following data is part of a premarket notification filed by Walter Lorenz Surgical, Inc. with the FDA for Lorenz 1.0mm, 1.5mm, 2.0mm System.
Device ID | K953385 |
510k Number | K953385 |
Device Name: | LORENZ 1.0MM, 1.5MM, 2.0MM SYSTEM |
Classification | Plate, Bone |
Applicant | WALTER LORENZ SURGICAL, INC. 1520 TRADEPORT DR. Jacksonville, FL 32218 -2480 |
Contact | W. Dutch Harrison |
Correspondent | W. Dutch Harrison WALTER LORENZ SURGICAL, INC. 1520 TRADEPORT DR. Jacksonville, FL 32218 -2480 |
Product Code | JEY |
CFR Regulation Number | 872.4760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-07-19 |
Decision Date | 1995-09-28 |