FDA Grants 510(k) Clearance to Stryker’s Sonopet 3

The US Food and Drug Administration has granted 510(k) clearance to Stryker for the Sonopet 3 surgical platform, according to Medical Device Network. The publisher describes Sonopet 3 as Stryker’s latest ultrasonic platform for bone and soft tissue removal.

The reported regulatory action concerns Stryker, which Medical Device Network identifies as a medical technology company. The clearance places Sonopet 3 among the company’s products with FDA 510(k) clearance reported by the publication.

FDA 510(k) clearance reported for Sonopet 3

Medical Device Network reported that the FDA granted the 510(k) clearance for Sonopet 3. The report identifies the device as a surgical platform and characterizes it as ultrasonic.

According to Medical Device Network, the platform is intended for bone and soft tissue removal. The supplied report does not provide further product specifications, procedural details, or additional clinical claims.

Key details for medical device sales professionals

For medical device sales professionals, the central development is the reported FDA 510(k) clearance for Stryker’s Sonopet 3 platform. The available information identifies both the regulatory action and the platform’s stated use.

• Company: Stryker
• Platform: Sonopet 3
• Regulatory action: FDA 510(k) clearance
• Platform type: Ultrasonic surgical platform
• Reported application: Bone and soft tissue removal

Medical Device Network describes Sonopet 3 as Stryker’s latest ultrasonic platform. Its report attributes the clearance to the US FDA and identifies bone and soft tissue removal as the platform’s stated focus.

Reported scope of the announcement

The announcement is a regulatory milestone centered on a specific Stryker surgical platform. Medical Device Network’s report provides the available details: FDA 510(k) clearance, the Sonopet 3 name, ultrasonic platform classification, and its reported application in bone and soft tissue removal.

No further details were included in the supplied evidence regarding product specifications or procedural use. Medical Device Network is the source for the reported clearance and the description of Sonopet 3.