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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K241466

Shoreline ACS Interbody System; Shoreline RT Interbody System; Regatta Lateral System; Reef L Interbody System; Reef TO/TA System; Meridian Interbody System; WaveForm C Interbody System; WaveForm L Interbody System; WaveForm TO Interbody System; WaveForm TA Interbody System; WaveForm A Interbody System · SeaSpine Orthopedics Corporation · decided 2024-06-20 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
REEF LRL2-100608Seaspine Orthopedics CorporationMAX OVD PHM10889981442187