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FDA 510(k)

VERITAS DRY COLLAGEN MATRIX, VERITAS DRY OR VERITAS PSD

K-Number: K041669 · 2004-10-27

ApplicantSynovis Surgical Innovations
Decision Date2004-10-27
Product CodeFTM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VERITAS DRY COLLAGEN MATRIX, VERITAS DRY OR VERITAS PSD is the device name listed in this FDA 510(k) record. The listed applicant is Synovis Surgical Innovations. It received FDA 510(k) clearance on 2004-10-27 under 510(k) number K041669. The device is classified under product code FTM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERITAS DRY COLLAGEN MATRIX, VERITAS DRY OR VERITAS PSD?

VERITAS DRY COLLAGEN MATRIX, VERITAS DRY OR VERITAS PSD is a medical device that received FDA 510(k) clearance on 2004-10-27. The listed applicant is Synovis Surgical Innovations. The 510(k) number is K041669.

When did VERITAS DRY COLLAGEN MATRIX, VERITAS DRY OR VERITAS PSD receive FDA 510(k) clearance?

VERITAS DRY COLLAGEN MATRIX, VERITAS DRY OR VERITAS PSD received FDA 510(k) clearance on 2004-10-27, under 510(k) number K041669.

Who is the listed applicant for VERITAS DRY COLLAGEN MATRIX, VERITAS DRY OR VERITAS PSD?

The FDA 510(k) record lists Synovis Surgical Innovations as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VERITAS DRY COLLAGEN MATRIX, VERITAS DRY OR VERITAS PSD?

The FDA product code for VERITAS DRY COLLAGEN MATRIX, VERITAS DRY OR VERITAS PSD is FTM.

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Other records listing Synovis Surgical Innovations 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.

K122306SYNOVIS COLLAGEN MATRIX (TBD)K083039VERITAS COLLAGEN MATRIX (DRY)K062915VERITAS COLLAGEN MATRIXK040415PERI-STRIPS STAPLE LINE REINFORCEMENT - SLEEVE AND STRIP CONFIGURATIONS - AND PERI-STRIPS DRY STAPLE LINE REINFORCEMENTK040119PERI-STRIPS STAPLE LINE REINFORCEMENT-SLEEVE CONFIGURATION, PERI-STRIPS STAPLE LINE REINFORCEMENT-STRIP CONFIGURATIONK040001STEERABLE STYLET

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Related Devices (Code: FTM)

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.

K262406EluPro Antibiotic-Eluting BioEnvelopeBoston ScientificK250598Endoform Reconstructive Template - PLGAAroa Biosurgery , Ltd.K243595OviTex PRS (Long-Term Resorbable)TELA Bio, Inc.K233991CanGaroo RM Antibacterial EnvelopeElutia, Inc.K241126OviTex PRSTELA Bio, Inc.K223052Peri-Guard and Supple Peri-GuardSynovis Life Technologies, Inc.

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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