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510(k) K853799

NEUROSURGICAL HEADREST by Cedar Surgical, Inc.

K853799 is an FDA 510(k) premarket notification submitted by Cedar Surgical, Inc. for the device "NEUROSURGICAL HEADREST". 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)
  • K864421 — RAYLOR(TM) PERIOSTEAL ELEVATORS (November 26, 1986)
  • K864424 — RAYLOR(TM) PROTECTIVE RETRACTOR (November 26, 1986)
  • K864426 — RAYLOR(TM) DEPTH GAUGE (November 26, 1986)
  • K864422 — RAYLOR(TM) MALLET (November 24, 1986)
  • K864423 — RAYLOR(TM) OSTEOTOMES (November 24, 1986)

FDA data resources