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FDA 510(k)

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

N.º K: K192615 · 2019-12-17

Fecha de decisión2019-12-17
Código de productoFTM
Comité asesorSU
DecisiónSubstantially Equivalent

Resumen del dispositivo

Peri-Strips Dry with Veritas Collagen Matrix with Secure Grip Technology (PSDV-SG) is the device name listed in this FDA 510(k) record. The listed applicant is Synovis Life Technologies, Inc. (Baxter International Inc.). It received FDA 510(k) clearance on 2019-12-17 under 510(k) number K192615. The device is classified under product code FTM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

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. The listed applicant is Synovis Life Technologies, Inc. (Baxter International Inc.). The 510(k) number is K192615.

When did Peri-Strips Dry with Veritas Collagen Matrix with Secure Grip Technology (PSDV-SG) receive FDA 510(k) clearance?

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

Who is the listed applicant for Peri-Strips Dry with Veritas Collagen Matrix with Secure Grip Technology (PSDV-SG)?

The FDA 510(k) record lists Synovis Life Technologies, Inc. (Baxter International Inc.) as the applicant. This does not by itself establish the device manufacturer.

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.

Ensayos clínicos relacionados

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

Dispositivos relacionados (Código: FTM)

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

Fuente oficial

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