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510(k) K962425

BONOPTY COAXIAL BONE BIOPSY SYSTEM WITH ECCENTRIC DRILL(10-1072,3,4) by Radi Medical Systems AB — Product Code GAA

K962425 is an FDA 510(k) premarket notification submitted by Radi Medical Systems AB for the device "BONOPTY COAXIAL BONE BIOPSY SYSTEM WITH ECCENTRIC DRILL(10-1072,3,4)". The FDA issued a decision of Substantially Equivalent on September 11, 1996. The device falls under product code GAA (Needle, Aspiration And Injection, Disposable), a Class I device regulated under 21 CFR 878.4800. Radi Medical Systems AB has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 11, 1996
Date Received
June 24, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Needle, Aspiration And Injection, Disposable
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type

Other clearances by Radi Medical Systems AB

  • K123984 — QUANTIEN MEASUREMENT SYSTEM (March 28, 2013)
  • K092105 — RADIANALYZER XPRESS (October 9, 2009)
  • K080813 — PRESSUREWIRE CERTUS, CERTUS (300CM), AERIS, AERIS (300CM), RECEIVER (July 1, 2008)
  • K080206 — MODIFICATION TO FEMOSTOP FEMORAL COMPRESSION SYSTEM (February 26, 2008)
  • K062769 — PRESSUREWIRE CERTUS, MODELS 12006 AND 12306 (December 4, 2006)
  • K042628 — MODIFICATION TO: RADIANALYZER, MODEL 12711 (January 19, 2005)
  • K033291 — TOPSEAL HEMOSTATIC DRESSING, MODEL 11150 (March 17, 2004)
  • K031662 — PRESSURE WIRE SENSOR, MODELS 12004/12304 (June 6, 2003)
  • K024107 — FEMOSTOP FEMORAL COMPRESSION SYSTEM (December 24, 2002)
  • K022188 — RADIANALYZER, MODEL 12710 (October 3, 2002)

Other clearances for product code GAA

  • K223625 — CapnoSpot™ Pneumothorax Decompression Indicator (March 28, 2023)
  • K102274 — ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENT (June 15, 2011)
  • K011586 — IRMA SL BLOOD ANALYSIS SYSTEM GL CARTRIDGE (November 16, 2001)
  • K994151 — PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICES (March 1, 2000)
  • K983200 — INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEX (December 11, 1998)
  • K974741 — MANAN ACCURA NEEDLE (January 8, 1998)
  • K961959 — MD TECH BIOPSY SET FOR BONE AND BONE MARROW (July 19, 1996)
  • K945109 — MONOJECT BONE MARROW BIOPSY TRAYS (November 14, 1994)
  • K940024 — MANAN GENERAL PURPOSE INTRODUCER NEEDLE (February 25, 1994)
  • K940025 — MANAN BONE MARROW HARVEST NEEDLES (February 25, 1994)

FDA data resources