The following data is part of a premarket notification filed by United States Surgical, A Division Of Tyco Healthc with the FDA for Polysorb Suture.
Device ID | K981935 |
510k Number | K981935 |
Device Name: | POLYSORB SUTURE |
Classification | Suture, Absorbable, Synthetic, Polyglycolic Acid |
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 | GAM |
CFR Regulation Number | 878.4493 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-06-02 |
Decision Date | 1998-06-25 |
Summary: | summary |