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510(k) K873684

ACE INTRA COMPARTMENTAL PRESSURE MONITOR by Ace Medical Co. — Product Code LXC

K873684 is an FDA 510(k) premarket notification submitted by Ace Medical Co. for the device "ACE INTRA COMPARTMENTAL PRESSURE MONITOR". The FDA issued a decision of Substantially Equivalent on January 20, 1988. The device falls under product code LXC (Monitor, Pressure, Intracompartmental), a Class U device. Ace Medical Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 20, 1988
Date Received
September 14, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Monitor, Pressure, Intracompartmental
Device Class
Class U
Regulation Number
Review Panel
OR
Submission Type

Other clearances by Ace Medical Co.

  • K200387 — Ace Medical Surgical Instruments (July 21, 2020)
  • K972183 — DEPUY ACE A.I.M. TITANIUM TIBIAL NAIL (August 26, 1997)
  • K955472 — ACE HUMERUS & RADIUS PLATES (April 1, 1996)
  • K955388 — ACE-DUPONT COMPOSITE RINGS (January 31, 1996)
  • K954485 — 6.5MM SOLID CANCELLOUS BONE SCREW (October 31, 1995)
  • K954069 — ACE CERVICAL TRACTION HALOZS, TONGS & PINS (October 12, 1995)
  • K950618 — ACE SUPRACONDYLAR PLATE (May 10, 1995)
  • K933968 — ACE PELVIC STABILIZER (June 16, 1994)
  • K931652 — ACE 6.5 MM BONE SCREW (April 28, 1994)
  • K930592 — ACE UNIVERSAL RECONSTRUCTION PLATE (July 26, 1993)

Other clearances for product code LXC

  • K251900 — MY01 Continuous Compartmental Pressure Monitor (January 16, 2026)
  • K242997 — MY01 Continuous Compartmental Pressure Monitor (March 13, 2025)
  • K223509 — Compremium Compartment Compressibility Monitoring System (CPM#1) (April 14, 2023)
  • K220952 — MY01 Continuous Compartmental Pressure Monitor (May 24, 2022)
  • K210525 — MY01 Continuous Compartmental Pressure Monitor (April 22, 2021)
  • K202635 — MY01 Continuous Compartmental Pressure Monitor (December 10, 2020)
  • K193321 — MY01 Continuous Compartmental Pressure Monitor (July 30, 2020)
  • K131966 — TWIN STAR EXTREMITY COMPARTMENT SYNDROME MONITOR AND FLUID COLLECTION CATHETER S (February 7, 2014)
  • K090961 — TWIN STAR COMPARTMENT PRESSURE MONITOR AND FLUID COLLECTION CATHETER SYSTEM (CMS (June 12, 2009)
  • K060963 — TWIN STAR COMPARTMENT PRESSURE MONITORING AND FLUID COLLECTION MONITOR (CMS MONI (June 6, 2006)

FDA data resources