The following data is part of a premarket notification filed by Lifecell Corp. with the FDA for Lrtm Surgical Mesh.
| Device ID | K070560 |
| 510k Number | K070560 |
| Device Name: | LRTM SURGICAL MESH |
| Classification | Mesh, Surgical |
| Applicant | LIFECELL CORP. ONE MILLENNIUM WAY Branchburg, NJ 08876 |
| Contact | Lorraine T Montemurro |
| Correspondent | Lorraine T Montemurro LIFECELL CORP. ONE MILLENNIUM WAY Branchburg, NJ 08876 |
| Product Code | FTM |
| CFR Regulation Number | 878.3300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-02-27 |
| Decision Date | 2007-06-11 |
| Summary: | summary |