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FDA 510(k)

VERITAS COLLAGEN MATRIX

K-Number: K062915 · 2006-12-06

ApplicantSynovis Surgical Innovations
Decision Date2006-12-06
Product CodeFTM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VERITAS COLLAGEN MATRIX 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 2006-12-06 under 510(k) number K062915. 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 COLLAGEN MATRIX?

VERITAS COLLAGEN MATRIX is a medical device that received FDA 510(k) clearance on 2006-12-06. The listed applicant is Synovis Surgical Innovations. The 510(k) number is K062915.

When did VERITAS COLLAGEN MATRIX receive FDA 510(k) clearance?

VERITAS COLLAGEN MATRIX received FDA 510(k) clearance on 2006-12-06, under 510(k) number K062915.

Who is the listed applicant for VERITAS COLLAGEN MATRIX?

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 COLLAGEN MATRIX?

The FDA product code for VERITAS COLLAGEN MATRIX 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)K041669VERITAS DRY COLLAGEN MATRIX, VERITAS DRY OR VERITAS PSDK040415PERI-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

View all 8 devices →

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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