The following data is part of a premarket notification filed by Walter Lorenz Surgical, Inc. with the FDA for Lorenz 1.5 Mm Neuro Pack/lorenz 2.0 Ft Plates.
| Device ID | K972322 |
| 510k Number | K972322 |
| Device Name: | LORENZ 1.5 MM NEURO PACK/LORENZ 2.0 FT PLATES |
| 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 | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-06-20 |
| Decision Date | 1997-08-18 |
| Summary: | summary |