The following data is part of a premarket notification filed by Surgical Specialties Corp. with the FDA for Modified Monoderm Monofilament, Synthetic, Absorbable Suture.
Device ID | K052437 |
510k Number | K052437 |
Device Name: | MODIFIED MONODERM MONOFILAMENT, SYNTHETIC, ABSORBABLE SUTURE |
Classification | Suture, Absorbable, Synthetic, Polyglycolic Acid |
Applicant | SURGICAL SPECIALTIES CORP. 100 DENNIS DR. Reading, PA 19606 |
Contact | Elizabeth Lazaro |
Correspondent | Elizabeth Lazaro SURGICAL SPECIALTIES CORP. 100 DENNIS DR. Reading, PA 19606 |
Product Code | GAM |
CFR Regulation Number | 878.4493 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-09-06 |
Decision Date | 2005-11-07 |
Summary: | summary |