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FDA 510(k)

CARESORB-Polyglactin 910 Surgical Suture, CARESORB-Polyglactin 910 (fast absorbing) Surgical Suture

K-Number: K170166 · 2017-09-29

Decision Date2017-09-29
Product CodeGAM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CARESORB-Polyglactin 910 Surgical Suture, CARESORB-Polyglactin 910 (fast absorbing) Surgical Suture is the device name listed in this FDA 510(k) record. The listed applicant is Cpt Sutures Co., Ltd.. It received FDA 510(k) clearance on 2017-09-29 under 510(k) number K170166. 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 CARESORB-Polyglactin 910 Surgical Suture, CARESORB-Polyglactin 910 (fast absorbing) Surgical Suture?

CARESORB-Polyglactin 910 Surgical Suture, CARESORB-Polyglactin 910 (fast absorbing) Surgical Suture is a medical device that received FDA 510(k) clearance on 2017-09-29. The listed applicant is Cpt Sutures Co., Ltd.. The 510(k) number is K170166.

When did CARESORB-Polyglactin 910 Surgical Suture, CARESORB-Polyglactin 910 (fast absorbing) Surgical Suture receive FDA 510(k) clearance?

CARESORB-Polyglactin 910 Surgical Suture, CARESORB-Polyglactin 910 (fast absorbing) Surgical Suture received FDA 510(k) clearance on 2017-09-29, under 510(k) number K170166.

Who is the listed applicant for CARESORB-Polyglactin 910 Surgical Suture, CARESORB-Polyglactin 910 (fast absorbing) Surgical Suture?

The FDA 510(k) record lists Cpt Sutures Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CARESORB-Polyglactin 910 Surgical Suture, CARESORB-Polyglactin 910 (fast absorbing) Surgical Suture?

The FDA product code for CARESORB-Polyglactin 910 Surgical Suture, CARESORB-Polyglactin 910 (fast absorbing) Surgical 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.

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.