Cleared Traditional

K971996 - MEDIVISION ARTHROSCOP

K971996 is an FDA 510(k) clearance for MEDIVISION ARTHROSCOP, manufactured by Medivision Scope Service Center, Inc.. The device is a Class 2 Orthopedic device with product code HRX cleared through the Traditional 510(k) pathway after a 62-day FDA review.

K971996 · Medivision Scope Service Center, Inc. · Orthopedic device
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Jul 1997
Decision
62d
Days
Class 2
Risk

K971996 is an FDA 510(k) clearance for the MEDIVISION ARTHROSCOP. Classified as Arthroscope (product code HRX), Class II - Special Controls.

Submitted by Medivision Scope Service Center, Inc. (Anaheim, US). The FDA issued a Cleared decision on July 31, 1997 after a review of 62 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 Medivision Scope Service Center, Inc. devices

FDA 510(k) Submission Details - K971996

510(k) Number K971996 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 30, 1997
Decision Date July 31, 1997
Days to Decision 62 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
60d faster than avg
Panel avg: 122d · This submission: 62d
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 480
Devices cleared under the same product code (HRX) and FDA review panel - the closest regulatory comparables to K971996.
TOTAL PERFORMANCE SYSTEM SHAVER
K973195 · Stryker Endoscopy · Oct 1997
BLACKSTONE MEDICAL, INC. LAPAROSCOPIC DISC REMOVAL SYSTEM
K972768 · Blackstone Medical, Inc. · Sep 1997
DYONICS DISPOSABLE ENDOSCOPIC SURGERY BLADES
K970511 · Smith & Nephew, Inc. · Aug 1997
LIMITED REUSE ENDOSCOPIC BLADES
K971676 · Smith & Nephew, Inc. · Jun 1997
ARTHROSCOPE
K971083 · Electro-Biology, Inc. · Jun 1997
UNIVERSAL DRIVE SYSTEM
K971059 · Linvatec Corp. · Jun 1997