Never miss a competitor's FDA clearance. FDA orthopedic 510(k) clearances for this applicant, in
chronological order. K-numbers link to the official FDA record.
1clearances tracked
2026-09-08first in this archive
2026-09-08most recent
1product codes
First clearance in this archive: 2026-09-08 —
K262341, b-ONE® Mobio Total Knee System Revision Cemented Tibial Augments, Stem Extensions and Press-Fit Stem Extensions.
Archive coverage is decisions 2026-08-26 to 2026-09-27; “first in this
archive” is scoped to that coverage and is not a claim about this
applicant’s first-ever FDA clearance.