Home / 510(k) Clearances / K760636

510(k) K760636

ORTHOMIX by Diemolding Corp. — Product Code JDZ

K760636 is an FDA 510(k) premarket notification submitted by Diemolding Corp. for the device "ORTHOMIX". The FDA issued a decision of Substantially Equivalent on October 5, 1976. The device falls under product code JDZ (Mixer, Cement, For Clinical Use), a Class I device regulated under 21 CFR 888.4210. Diemolding Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 5, 1976
Date Received
September 13, 1976
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mixer, Cement, For Clinical Use
Device Class
Class I
Regulation Number
888.4210
Review Panel
OR
Submission Type

Other clearances by Diemolding Corp.

  • K962749 — THERAPEP W/MOUTHPIECE, W/PEDIATRIC MASK, W/SMALL MASK, W/LARGE MASK, RESISTOR/PO (October 10, 1996)
  • K961455 — MEDSHIELD/AEROCHAMBER (July 25, 1996)
  • K902713 — ACCESS. KIT FOR THE BIOSURGE SYNCHRONOUS AUTOTRANS (July 25, 1990)
  • K902114 — CUFF-MATE 2 ENDOTRACHEAL CUFF INFLATOR & MONITOR (July 18, 1990)
  • K900754 — RESPIREX 2 (March 15, 1990)
  • K893791 — BREATHING MOUTHPIECE (June 23, 1989)
  • K781759 — RESCAL (November 27, 1978)
  • K780750 — O2 CONNECTOR (July 27, 1978)
  • K770369 — VACON TM (March 1, 1977)
  • K760931 — I.V. DRIP MONITOR ALARM DEVICE, MONIFLO (January 5, 1977)

Other clearances for product code JDZ

  • K934253 — EXACTECH ALL POLY ACETABULAR CUP (April 29, 1994)
  • K925025 — PRISM BONE CEMENT MIXING SYSTEM (January 5, 1994)
  • K912190 — STRYKER HIGH VACUUM BONE CEMENT MIXER/INJECT SYST (August 29, 1991)
  • K892937 — REUSABLE BOWL AND SPATULA FOR MIXING BONE CEMENTS (June 22, 1989)
  • K861086 — ZIMMER VACUUM MIXING SYSTEM (April 14, 1986)
  • K854077 — MIX EVAC II (January 31, 1986)
  • K853310 — SIMPLEX ENHANCEMENT MIXER (September 11, 1985)
  • K851205 — CEMENTRIFUGE (July 16, 1985)
  • K843219 — ZIMMER BONE CEMENT CENTRIFUGATION SYS (November 29, 1984)
  • K792186 — HOWMEDICA MIX-KIT II (December 5, 1979)

FDA data resources