The following data is part of a premarket notification filed by United States Surgical, A Division Of Tyco Healthc with the FDA for Monofilament Biosyn Suture.
| Device ID | K000037 |
| 510k Number | K000037 |
| Device Name: | MONOFILAMENT BIOSYN SUTURE |
| Classification | Suture, Absorbable, Synthetic, Polyglycolic Acid |
| Applicant | UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC 150 GLOVER AVE. Norwalk, CT 06856 |
| Contact | Seth A Schulman |
| Correspondent | Seth A Schulman UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC 150 GLOVER AVE. Norwalk, CT 06856 |
| Product Code | GAM |
| CFR Regulation Number | 878.4493 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-01-06 |
| Decision Date | 2000-03-30 |