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510(k) K853800

UPPER-CHEST-SUPPORT CUSHION FOR OPERATIONS IN SITT by Cedar Surgical, Inc.

K853800 is an FDA 510(k) premarket notification submitted by Cedar Surgical, Inc. for the device "UPPER-CHEST-SUPPORT CUSHION FOR OPERATIONS IN SITT". The FDA issued a decision of Substantially Equivalent on October 7, 1985. Cedar Surgical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 7, 1985
Date Received
September 11, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Cedar Surgical, Inc.

  • K873692 — RAYLOR(TM) DRILL STOP (December 17, 1987)
  • K872281 — RAYLOR FUSION FUNNEL (November 2, 1987)
  • K873690 — CEDAR(TM) PELVIC CUSHION (October 26, 1987)
  • K873691 — CEDAR(TM) RETRACTOR RING (September 28, 1987)
  • K864425 — RAYLOR(TM) DISSECTING HOOK (December 12, 1986)
  • K864424 — RAYLOR(TM) PROTECTIVE RETRACTOR (November 26, 1986)
  • K864426 — RAYLOR(TM) DEPTH GAUGE (November 26, 1986)
  • K864421 — RAYLOR(TM) PERIOSTEAL ELEVATORS (November 26, 1986)
  • K864422 — RAYLOR(TM) MALLET (November 24, 1986)
  • K864423 — RAYLOR(TM) OSTEOTOMES (November 24, 1986)

FDA data resources