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 |