The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Modification To Versabond Bone Cement.
| Device ID | K033509 |
| 510k Number | K033509 |
| Device Name: | MODIFICATION TO VERSABOND BONE CEMENT |
| Classification | Bone Cement |
| Applicant | SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 |
| Contact | David Henley |
| Correspondent | David Henley SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 |
| Product Code | LOD |
| CFR Regulation Number | 888.3027 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-11-06 |
| Decision Date | 2003-11-28 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 23596010494720 | K033509 | 000 |