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FDA 510(k)

GRAMSORB SYNTHETIC ABSORBABLE SUTURE

K-Number: K003017 · 2001-03-13

ApplicantGramsmed, LLC
Decision Date2001-03-13
Product CodeGAM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GRAMSORB SYNTHETIC ABSORBABLE SUTURE is the device name listed in this FDA 510(k) record. The listed applicant is Gramsmed, LLC. It received FDA 510(k) clearance on 2001-03-13 under 510(k) number K003017. The device is classified under product code GAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRAMSORB SYNTHETIC ABSORBABLE SUTURE?

GRAMSORB SYNTHETIC ABSORBABLE SUTURE is a medical device that received FDA 510(k) clearance on 2001-03-13. The listed applicant is Gramsmed, LLC. The 510(k) number is K003017.

When did GRAMSORB SYNTHETIC ABSORBABLE SUTURE receive FDA 510(k) clearance?

GRAMSORB SYNTHETIC ABSORBABLE SUTURE received FDA 510(k) clearance on 2001-03-13, under 510(k) number K003017.

Who is the listed applicant for GRAMSORB SYNTHETIC ABSORBABLE SUTURE?

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

What is the FDA product code for GRAMSORB SYNTHETIC ABSORBABLE SUTURE?

The FDA product code for GRAMSORB SYNTHETIC ABSORBABLE SUTURE is GAM.

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 Gramsmed, LLC 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 7 devices →

Related Devices (Code: GAM)

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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