The following data is part of a premarket notification filed by United States Surgical, A Division Of Tyco Healthc with the FDA for Sofsilk Suture.
Device ID | K981128 |
510k Number | K981128 |
Device Name: | SOFSILK SUTURE |
Classification | Suture, Nonabsorbable, Silk |
Applicant | UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC 150 GLOVER AVE. Norwalk, CT 06856 |
Contact | Jamie Yieh |
Correspondent | Jamie Yieh UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC 150 GLOVER AVE. Norwalk, CT 06856 |
Product Code | GAP |
CFR Regulation Number | 878.5030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-03-30 |
Decision Date | 1998-05-11 |