Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Cedar Surgical, Inc. — Predicate Candidate Screening

17 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

26 daysmedian FDA review time

100 days90th percentile

17clearances measured

K-number	Device	Applicant	Decided	Review days
K873692	RAYLOR(TM) DRILL STOP	Cedar Surgical, Inc.	1987-12-17	100
K872281	RAYLOR FUSION FUNNEL	Cedar Surgical, Inc.	1987-11-02	139
K873690	CEDAR(TM) PELVIC CUSHION	Cedar Surgical, Inc.	1987-10-26	48
K873691	CEDAR(TM) RETRACTOR RING	Cedar Surgical, Inc.	1987-09-28	20
K864425	RAYLOR(TM) DISSECTING HOOK	Cedar Surgical, Inc.	1986-12-12	32
K864426	RAYLOR(TM) DEPTH GAUGE	Cedar Surgical, Inc.	1986-11-26	16
K864424	RAYLOR(TM) PROTECTIVE RETRACTOR	Cedar Surgical, Inc.	1986-11-26	16
K864421	RAYLOR(TM) PERIOSTEAL ELEVATORS	Cedar Surgical, Inc.	1986-11-26	16
K864422	RAYLOR(TM) MALLET	Cedar Surgical, Inc.	1986-11-24	14
K864423	RAYLOR(TM) OSTEOTOMES	Cedar Surgical, Inc.	1986-11-24	14
K863416	RAYLOR MINI-PROBE	Cedar Surgical, Inc.	1986-09-24	21
K863415	RAYLOR BONE IMPACTORS	Cedar Surgical, Inc.	1986-09-24	21
K853797	KNEELING ATTACHMENT & CUSHIONED FACE REST SYS FOR	Cedar Surgical, Inc.	1985-10-07	26
K853800	UPPER-CHEST-SUPPORT CUSHION FOR OPERATIONS IN SITT	Cedar Surgical, Inc.	1985-10-07	26
K853799	NEUROSURGICAL HEADREST	Cedar Surgical, Inc.	1985-10-07	26
K853796	RAYLOR RETRACTORS	Cedar Surgical, Inc.	1985-10-07	26
K853798	BONE IMPACTORS	Cedar Surgical, Inc.	1985-10-07	26

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda