ANVIL RETRACTOR

Retractor

TWIN CITY SURGICAL, INC.

The following data is part of a premarket notification filed by Twin City Surgical, Inc. with the FDA for Anvil Retractor.

Pre-market Notification Details

Device IDK830585
510k NumberK830585
Device Name:ANVIL RETRACTOR
ClassificationRetractor
Applicant TWIN CITY SURGICAL, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeGAD  
CFR Regulation Number878.4800 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1983-02-23
Decision Date1983-05-27

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.