Home / 510(k) Clearances / K781450

510(k) K781450

DRIVERS by Orthopedic Equipment Co., Inc. — Product Code GFC

K781450 is an FDA 510(k) premarket notification submitted by Orthopedic Equipment Co., Inc. for the device "DRIVERS". The FDA issued a decision of Substantially Equivalent on September 27, 1978. The device falls under product code GFC (Driver, Surgical, Pin), a Class I device regulated under 21 CFR 878.4820. Orthopedic Equipment Co., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 27, 1978
Date Received
August 23, 1978
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Driver, Surgical, Pin
Device Class
Class I
Regulation Number
878.4820
Review Panel
SU
Submission Type

Other clearances by Orthopedic Equipment Co., Inc.

  • K834035 — UNIVERSAL SELF-ALIGNING ACETABULAR COM (June 19, 1984)
  • K841189 — OEC/REZAIAN SPINAL FIXATOR (May 16, 1984)
  • K800530 — SCHLEIN TRI-SURFACE ANKLE (April 2, 1980)
  • K781445 — SPREADER (September 27, 1979)
  • K790247 — TOURNIQUET TEST GAGE (February 26, 1979)
  • K790209 — FILTER SYSTEM, ALTNER DISPOSABLE (February 26, 1979)
  • K781444 — OUTRIGGER DISTRACTION UNIT (September 27, 1978)
  • K781446 — C RING CLINCHER (September 27, 1978)
  • K781448 — HARRINGTON HOOK CLAMP (September 27, 1978)
  • K781447 — THREADED ROD CLAMP (September 27, 1978)

Other clearances for product code GFC

  • K780255 — NEEDLE DRIVER (April 18, 1978)

FDA data resources