Cleared Traditional

K904720 - POWERCUT SURGICAL SYSTEM

K904720 is the FDA 510(k) clearance for POWERCUT SURGICAL SYSTEM by Baxter Healthcare Corp. It is a Class 2 Orthopedic device (product code HRX) cleared through the Traditional 510(k) pathway after a 8-day FDA review.

K904720 · Baxter Healthcare Corp · Orthopedic device
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Oct 1990
Decision
8d
Days
Class 2
Risk

K904720 is an FDA 510(k) clearance for the POWERCUT SURGICAL SYSTEM, BLADES, AND ACCESSORIES. Classified as Arthroscope (product code HRX), Class II - Special Controls.

Submitted by Baxter Healthcare Corp (Santa Ana, US). The FDA issued a Cleared decision on October 26, 1990 after a review of 8 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 Baxter Healthcare Corp devices

Submission Details

510(k) Number K904720 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 18, 1990
Decision Date October 26, 1990
Days to Decision 8 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
114d faster than avg
Panel avg: 122d · This submission: 8d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 376
Devices cleared under the same product code (HRX) and FDA review panel - the closest regulatory comparables to K904720.
STRYKER ARTHROSCOPIC INFUSION PUMP
K910858 · Stryker Corp. · May 1991
MICROSURGICAL INSTRUMENTS
K911300 · Danek Medical, Inc. · Apr 1991
MOTOR DRIVEN EXTIRPATION INSTRUMENTS
K904859 · Aesculap, Inc. · Mar 1991
SHEPPERD LUMBAR DISCECTOMY SYSTEM
K900608 · Downs Surgical , Ltd. · Oct 1990
SHEPPERD STRAIGHT AND CURVED NEEDLES
K900609 · Downs Surgical , Ltd. · Oct 1990
SHEPPERD CANNULA STILLETTE & OBDURATOR SET
K900610 · Downs Surgical , Ltd. · Oct 1990