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FDA 510(k)

SILKAM NONABSORBABLE SILK SURGICAL SUTURE

K-Number: K990089 · 1999-03-15

Decision Date1999-03-15
Product CodeGAP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SILKAM NONABSORBABLE SILK SURGICAL SUTURE is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1999-03-15 under 510(k) number K990089. The device is classified under product code GAP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILKAM NONABSORBABLE SILK SURGICAL SUTURE?

SILKAM NONABSORBABLE SILK SURGICAL SUTURE is a medical device that received FDA 510(k) clearance on 1999-03-15. The listed applicant is Aesculap, Inc.. The 510(k) number is K990089.

When did SILKAM NONABSORBABLE SILK SURGICAL SUTURE receive FDA 510(k) clearance?

SILKAM NONABSORBABLE SILK SURGICAL SUTURE received FDA 510(k) clearance on 1999-03-15, under 510(k) number K990089.

Who is the listed applicant for SILKAM NONABSORBABLE SILK SURGICAL SUTURE?

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

What is the FDA product code for SILKAM NONABSORBABLE SILK SURGICAL SUTURE?

The FDA product code for SILKAM NONABSORBABLE SILK SURGICAL SUTURE is GAP.

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 Aesculap, 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 195 devices →

Related Devices (Code: GAP)

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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