Cleared Traditional

K872544 - IRRIGATION PRESSURE MONITOR

K872544 is an FDA 510(k) clearance for IRRIGATION PRESSURE MONITOR, manufactured by Avec Scientific Design Corp.. The device is a Class 2 Orthopedic device with product code HRX cleared through the Traditional 510(k) pathway after a 67-day FDA review.

K872544 · Avec Scientific Design Corp. · Orthopedic device
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Sep 1987
Decision
67d
Days
Class 2
Risk

K872544 is an FDA 510(k) clearance for the IRRIGATION PRESSURE MONITOR. Classified as Arthroscope (product code HRX), Class II - Special Controls.

Submitted by Avec Scientific Design Corp. (Philadelphia, US). The FDA issued a Cleared decision on September 4, 1987 after a review of 67 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.1100 - the FDA orthopedic device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Avec Scientific Design Corp. devices

FDA 510(k) Submission Details - K872544

510(k) Number K872544 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 29, 1987
Decision Date September 04, 1987
Days to Decision 67 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
55d faster than avg
Panel avg: 122d · This submission: 67d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HRX Device Classification - Class 2, Special Controls

Product Code HRX Arthroscope
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.1100
Definition Validated Reprocessing Instructions And Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission If The Device Is Reusable And Has Specific Design Features (please Refer To Table 2 Of 82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf).
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Orthopedic devices follow this clearance model.

Regulatory Peers - HRX Arthroscope

All 539
Devices cleared under the same product code (HRX) and FDA review panel - the closest regulatory comparables to K872544.
C-O-T SET (CANNULA, OBTURATOR AND TROCAR) #TM-1360
K873650 · Arthropedics, Inc. · Nov 1987
MODEL 28200C/SHOULDER/ANKLE/ELBOW/HIP/TMJ/SM JOINT
K872986 · KARL STORZ Endoscopy-America, Inc. · Oct 1987
CONCEPT ARTHROSCOPIC PORTAL ROD
K873030 · Concept, Inc. · Sep 1987
THE KARL STORZ MODEL 28805 ARTHRO PUMP
K871621 · KARL STORZ Endoscopy-America, Inc. · Jun 1987
EFER ARTHROSCOPE
K870654 · Roseburg SA · May 1987
SIMPULSE ARTHROSCOPY IRRIGATION SYSTEM
K870915 · C.R. Bard, Inc. · Apr 1987