The following data is part of a premarket notification filed by Howmedica Corp. with the FDA for Universal Compression Screw.
| Device ID | K904809 |
| 510k Number | K904809 |
| Device Name: | UNIVERSAL COMPRESSION SCREW |
| Classification | Screw, Fixation, Bone |
| Applicant | HOWMEDICA CORP. 359 VETERANS BLVD. Rutherford, NJ 07070 |
| Contact | Robert E Smith |
| Correspondent | Robert E Smith HOWMEDICA CORP. 359 VETERANS BLVD. Rutherford, NJ 07070 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent For Some Indications (SN) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-10-24 |
| Decision Date | 1991-06-28 |