Skip to content
Scan

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

Clearance record K103712

GRYPHON PEEK DS ANCHOR W/ ORTHOCORD, GRYPHON PEEK ANCHOR W/ ORTHOCORD · Depuy Mitek, A Johnson & Johnson Company · decided 2011-03-11 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
GRYPHON ORTHOCORD210031Medos International SàrlHTY HWC JDR MAI MBI10886705019946
GRYPHON ORTHOCORD210030Medos International SàrlHTY HWC JDR MAI MBI10886705019939