Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

STAINLESS STEEL SUTURES, FLEXON STEEL SUTURES (STAINLESS)

K-Number: K955723 · 1996-02-27

Decision Date1996-02-27
Product CodeGAQ
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

STAINLESS STEEL SUTURES, FLEXON STEEL SUTURES (STAINLESS) is the device name listed in this FDA 510(k) record. The listed applicant is Davis & Geck, Inc.. It received FDA 510(k) clearance on 1996-02-27 under 510(k) number K955723. The device is classified under product code GAQ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the STAINLESS STEEL SUTURES, FLEXON STEEL SUTURES (STAINLESS)?

STAINLESS STEEL SUTURES, FLEXON STEEL SUTURES (STAINLESS) is a medical device that received FDA 510(k) clearance on 1996-02-27. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K955723.

When did STAINLESS STEEL SUTURES, FLEXON STEEL SUTURES (STAINLESS) receive FDA 510(k) clearance?

STAINLESS STEEL SUTURES, FLEXON STEEL SUTURES (STAINLESS) received FDA 510(k) clearance on 1996-02-27, under 510(k) number K955723.

Who is the listed applicant for STAINLESS STEEL SUTURES, FLEXON STEEL SUTURES (STAINLESS)?

The FDA 510(k) record lists Davis & Geck, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STAINLESS STEEL SUTURES, FLEXON STEEL SUTURES (STAINLESS)?

The FDA product code for STAINLESS STEEL SUTURES, FLEXON STEEL SUTURES (STAINLESS) is GAQ.

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.

Other records listing Davis & Geck, Inc. as applicant

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.

View all 45 devices →

Related Devices (Code: GAQ)

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.

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.

↑