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510(k) K931847

BIO-PREP CEMENT RESTRICTOR by Biomedical Devices, Inc. — Product Code LZN

K931847 is an FDA 510(k) premarket notification submitted by Biomedical Devices, Inc. for the device "BIO-PREP CEMENT RESTRICTOR". The FDA issued a decision of Substantially Equivalent on June 28, 1994. The device falls under product code LZN (Cement Obturator), a Class II device regulated under 21 CFR 878.3300. Biomedical Devices, Inc. has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 28, 1994
Date Received
April 13, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cement Obturator
Device Class
Class II
Regulation Number
878.3300
Review Panel
OR
Submission Type

Other clearances by Biomedical Devices, Inc.

  • K955439 — THE REEL THING (MODIFICATION) (December 26, 1995)
  • K931846 — BIO-PREP (January 21, 1994)
  • K925982 — BMD AIR/OXYGEN BLENDER (October 7, 1993)
  • K903533 — STERI-SHIELD (October 19, 1990)
  • K902677 — STERI-SHIELD (August 17, 1990)
  • K830605 — PUMP PALL AMBULATORY INSULIN INFUSION (March 31, 1983)

Other clearances for product code LZN

  • K220838 — Artisan Bone Plug, Universal Cement Restrictor (May 20, 2022)
  • K061824 — TORNIER CEMENT RESTRICTOR (September 14, 2006)
  • K032685 — CEMSTOP CEMENT RESTRICTOR (November 26, 2003)
  • K023680 — BIOBUCK CEMENT RESTRICTOR (November 19, 2002)
  • K011943 — IMPRO VISE ABSORBABLE CEMENT FLOW RESTRICTOR (September 19, 2001)
  • K010840 — SYNPLUG (April 20, 2001)
  • K993841 — CEMSTOP CEMENT RESTRICTOR (May 4, 2000)
  • K000587 — SHUTTLE STOP (May 4, 2000)
  • K992462 — OSTEONICS UNIVERSAL DISTAL CEMENT PLUG (August 13, 1999)
  • K972411 — LINK CEMENT PLUG (August 29, 1997)

FDA data resources