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FDA 510(k)

NONABSORBABLE POLYPROPYLENE SURGICAL SUTURE*

K-Number: K902872 · 1990-09-27

Decision Date1990-09-27
Product CodeGAW
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

NONABSORBABLE POLYPROPYLENE SURGICAL SUTURE* is the device name listed in this FDA 510(k) record. The listed applicant is United States Surgical, A Division of Tyco Healthc. It received FDA 510(k) clearance on 1990-09-27 under 510(k) number K902872. The device is classified under product code GAW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the NONABSORBABLE POLYPROPYLENE SURGICAL SUTURE*?

NONABSORBABLE POLYPROPYLENE SURGICAL SUTURE* is a medical device that received FDA 510(k) clearance on 1990-09-27. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K902872.

When did NONABSORBABLE POLYPROPYLENE SURGICAL SUTURE* receive FDA 510(k) clearance?

NONABSORBABLE POLYPROPYLENE SURGICAL SUTURE* received FDA 510(k) clearance on 1990-09-27, under 510(k) number K902872.

Who is the listed applicant for NONABSORBABLE POLYPROPYLENE SURGICAL SUTURE*?

The FDA 510(k) record lists United States Surgical, A Division of Tyco Healthc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NONABSORBABLE POLYPROPYLENE SURGICAL SUTURE*?

The FDA product code for NONABSORBABLE POLYPROPYLENE SURGICAL SUTURE* is GAW.

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 United States Surgical, A Division of Tyco Healthc 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 218 devices →

Related Devices (Code: GAW)

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

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

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