Cedar Surgical, Inc.
Cedar Surgical, Inc. holds FDA 510(k) medical device clearances, first cleared 1985, most recent 1987.
Top product codes for Cedar Surgical, Inc.
Recent clearances by Cedar Surgical, Inc.
- K873692 — RAYLOR(TM) DRILL STOP
- K872281 — RAYLOR FUSION FUNNEL
- K873690 — CEDAR(TM) PELVIC CUSHION
- K873691 — CEDAR(TM) RETRACTOR RING
- K864425 — RAYLOR(TM) DISSECTING HOOK
- K864421 — RAYLOR(TM) PERIOSTEAL ELEVATORS
- K864424 — RAYLOR(TM) PROTECTIVE RETRACTOR
- K864426 — RAYLOR(TM) DEPTH GAUGE
- K864422 — RAYLOR(TM) MALLET
- K864423 — RAYLOR(TM) OSTEOTOMES
- K863415 — RAYLOR BONE IMPACTORS
- K863416 — RAYLOR MINI-PROBE
- K853796 — RAYLOR RETRACTORS
- K853797 — KNEELING ATTACHMENT & CUSHIONED FACE REST SYS FOR
- K853798 — BONE IMPACTORS
- K853799 — NEUROSURGICAL HEADREST
- K853800 — UPPER-CHEST-SUPPORT CUSHION FOR OPERATIONS IN SITT
Data sourced from openFDA. This site is unofficial and independent of the FDA.