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

FDA 510(k)

Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture

K-Number: K151165 · 2016-02-17

Decision Date2016-02-17
Product CodeGAR
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture is a medical device manufactured by Aesculap, Inc.. It received FDA 510(k) clearance on 2016-02-17 under approval number K151165. The device is classified under product code GAR. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture?

Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture is a medical device that received FDA 510(k) clearance on 2016-02-17. It is manufactured by Aesculap, Inc.. The 510(k) number is K151165.

When was Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture approved by the FDA?

Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture received FDA 510(k) clearance on 2016-02-17, under approval number K151165.

What company makes Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture?

Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture is manufactured by Aesculap, Inc..

What is the FDA product code for Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture?

The FDA product code for Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture is GAR.

Related Clinical Trials

Other Devices by Aesculap, Inc.

View all 34 devices →

Related Devices (Code: GAR)

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.