FDA 510(k)

VENTRAL WALL DEFECT REDUCTION SILO

K-Number: K973082 · 1997-11-04

ApplicantSpecialty Surgical Products, Inc.

Decision Date1997-11-04

Product CodeFTL

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

VENTRAL WALL DEFECT REDUCTION SILO is the device name listed in this FDA 510(k) record. The listed applicant is Specialty Surgical Products, Inc.. It received FDA 510(k) clearance on 1997-11-04 under 510(k) number K973082. The device is classified under product code FTL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTRAL WALL DEFECT REDUCTION SILO?

VENTRAL WALL DEFECT REDUCTION SILO is a medical device that received FDA 510(k) clearance on 1997-11-04. The listed applicant is Specialty Surgical Products, Inc.. The 510(k) number is K973082.

When did VENTRAL WALL DEFECT REDUCTION SILO receive FDA 510(k) clearance?

VENTRAL WALL DEFECT REDUCTION SILO received FDA 510(k) clearance on 1997-11-04, under 510(k) number K973082.

Who is the listed applicant for VENTRAL WALL DEFECT REDUCTION SILO?

The FDA 510(k) record lists Specialty Surgical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENTRAL WALL DEFECT REDUCTION SILO?

The FDA product code for VENTRAL WALL DEFECT REDUCTION SILO is FTL.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Specialty Surgical Products, Inc. as applicant

K984106MAMMARY SIZER, MAMMARY PROTHESIS SIZER K983015VIRILIS PENILE PROSTHESIS K982258MAMMARY SIZER K982065STERILE SILICONE EXTERNAL WOUND COVER K982067MAGNETIC PORT SILICONE TISSUE EXPANDER K974653SILICONE ELASTOMER SHEETING

View all 11 devices →

Related Devices (Code: FTL)

K253956ProGrip™ advanced self-gripping polypropylene mesh (ADG1510, ADG2015, ADG3020, ADG4030)Sofradim Production K253125Parietene™ Flat Sheet MeshMedtronic - Sofradim Production K251955Onflex™ MeshDavol Inc., Subsidiary of C. R. Bard, Inc.K251557Bard® Mesh; Bard® Mesh Pre-ShapedDavol, Inc.K250869Parietene™ Macroporous Mesh (PPM5050 )Sofradim Production K250098Bard Soft Mesh; Bard Soft Mesh Pre-ShapedDavol, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.