Cleared Traditional

K910587 - MINISCOPE

K910587 is an FDA 510(k) clearance for MINISCOPE, manufactured by Citation Medical Corp.. The device is a Class 2 Orthopedic device with product code HRX cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K910587 · Citation Medical Corp. · Orthopedic device
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May 1991
Decision
90d
Days
Class 2
Risk

K910587 is an FDA 510(k) clearance for the MINISCOPE. Classified as Arthroscope (product code HRX), Class II - Special Controls.

Submitted by Citation Medical Corp. (Reno, US). The FDA issued a Cleared decision on May 13, 1991 after a review of 90 days - within the typical 510(k) review window.

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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Orthopedic review framework, consistent with the majority of Class II 510(k) submissions.

View all Citation Medical Corp. devices

FDA 510(k) Submission Details - K910587

510(k) Number K910587 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 12, 1991
Decision Date May 13, 1991
Days to Decision 90 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
32d faster than avg
Panel avg: 122d · This submission: 90d
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 552
Devices cleared under the same product code (HRX) and FDA review panel - the closest regulatory comparables to K910587.
INSIDE JOB
K912871 · 3M Health Care, Ltd. · Aug 1991
ARTHROSCOPY INSTRUMENT CANNULA
K911205 · Davol, Inc. · Jun 1991
STRYKER ARTHROSCOPIC INFUSION PUMP
K910858 · Stryker Corp. · May 1991
FLEXMEDICS MALLEABLE CANNULA
K910674 · Flexmedics · Apr 1991
MICROSURGICAL INSTRUMENTS
K911300 · Danek Medical, Inc. · Apr 1991
MOTOR DRIVEN EXTIRPATION INSTRUMENTS
K904859 · Aesculap, Inc. · Mar 1991