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FDA 510(k)

Peri-Strips Dry with Veritas Collagen Matrix with Secure Grip Technology (PSDV-SG)

K-Number: K192615 · 2019-12-17

Decision Date2019-12-17
Product CodeFTM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Peri-Strips Dry with Veritas Collagen Matrix with Secure Grip Technology (PSDV-SG) is a medical device manufactured by Synovis Life Technologies, Inc. (Baxter International Inc.). It received FDA 510(k) clearance on 2019-12-17 under approval number K192615. 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 Peri-Strips Dry with Veritas Collagen Matrix with Secure Grip Technology (PSDV-SG)?

Peri-Strips Dry with Veritas Collagen Matrix with Secure Grip Technology (PSDV-SG) is a medical device that received FDA 510(k) clearance on 2019-12-17. It is manufactured by Synovis Life Technologies, Inc. (Baxter International Inc.). The 510(k) number is K192615.

When was Peri-Strips Dry with Veritas Collagen Matrix with Secure Grip Technology (PSDV-SG) approved by the FDA?

Peri-Strips Dry with Veritas Collagen Matrix with Secure Grip Technology (PSDV-SG) received FDA 510(k) clearance on 2019-12-17, under approval number K192615.

What company makes Peri-Strips Dry with Veritas Collagen Matrix with Secure Grip Technology (PSDV-SG)?

Peri-Strips Dry with Veritas Collagen Matrix with Secure Grip Technology (PSDV-SG) is manufactured by Synovis Life Technologies, Inc. (Baxter International Inc.).

What is the FDA product code for Peri-Strips Dry with Veritas Collagen Matrix with Secure Grip Technology (PSDV-SG)?

The FDA product code for Peri-Strips Dry with Veritas Collagen Matrix with Secure Grip Technology (PSDV-SG) is FTM.

Related Clinical Trials

Related Devices (Code: FTM)

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.