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FDA 510(k)

MODIFIED COATED VICRYL* RAPIDE (POLYGLACTIN 910) SUTURE

K-Number: K033746 · 2003-12-18

ApplicantETHICON, Inc.
Decision Date2003-12-18
Product CodeGAM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODIFIED COATED VICRYL* RAPIDE (POLYGLACTIN 910) SUTURE is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 2003-12-18 under 510(k) number K033746. 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 MODIFIED COATED VICRYL* RAPIDE (POLYGLACTIN 910) SUTURE?

MODIFIED COATED VICRYL* RAPIDE (POLYGLACTIN 910) SUTURE is a medical device that received FDA 510(k) clearance on 2003-12-18. The listed applicant is ETHICON, Inc.. The 510(k) number is K033746.

When did MODIFIED COATED VICRYL* RAPIDE (POLYGLACTIN 910) SUTURE receive FDA 510(k) clearance?

MODIFIED COATED VICRYL* RAPIDE (POLYGLACTIN 910) SUTURE received FDA 510(k) clearance on 2003-12-18, under 510(k) number K033746.

Who is the listed applicant for MODIFIED COATED VICRYL* RAPIDE (POLYGLACTIN 910) SUTURE?

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

What is the FDA product code for MODIFIED COATED VICRYL* RAPIDE (POLYGLACTIN 910) SUTURE?

The FDA product code for MODIFIED COATED VICRYL* RAPIDE (POLYGLACTIN 910) SUTURE is GAM.

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Other records listing ETHICON, 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.

K253394Coated VICRYL™ (Polyglactin 910) Plus Antibacterial SutureK252047STRATAFIX™ Symmetric PDS™ Plus Knotless Tissue Control DevicesK253572STRATAFIX™ Spiral PRONOVA™ Unidirectional Knotless Tissue Control Device STRATAFIX™ Spiral PRONOVA™ Bidirectional Knotless Tissue Control DeviceK253852MONOCRYL™ Plus Antibacterial Poliglecaprone – 25 (Monofilament), Sterile Synthetic Absorbable Surgical SutureK252743STRATAFIX™ Spiral PDS™ Plus Knotless Tissue Control Device; STRATAFIX™ Spiral MONOCRYL™ Plus Knotless Tissue Control DeviceK243897PDS™ Plus Antibacterial (Polydioxanone) Sterile Synthetic Absorbable Surgical Suture

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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.

K253394Coated VICRYL™ (Polyglactin 910) Plus Antibacterial SutureETHICON, Inc.K253530Trexon™ Monofilament Synthetic Absorbable SutureMedtronicK253852MONOCRYL™ Plus Antibacterial Poliglecaprone – 25 (Monofilament), Sterile Synthetic Absorbable Surgical SutureETHICON, Inc.K252743STRATAFIX™ Spiral PDS™ Plus Knotless Tissue Control Device; STRATAFIX™ Spiral MONOCRYL™ Plus Knotless Tissue Control DeviceETHICON, Inc.K253620TroClose 1200Gordian Surgical, Ltd.K252820PGLA90 Poly(glycolide-co-L-lactide) Surgical Sutures (Calypso); PGLA90 Poly(glycolide-co-L-lactide) Surgical Sutures (Odysseus)Internacional Farmacéutica S.A DE C.V

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.

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