Cleared Traditional

K961853 - PROLINE FAST PASS ARTHOSCOPIC NEEDLE PASSER

K961853 is an FDA 510(k) clearance for PROLINE FAST PASS ARTHOSCOPIC NEEDLE PASSER, manufactured by Acufex Microsurgical, Inc.. The device is a Class 2 General & Plastic Surgery device with product code HRX cleared through the Traditional 510(k) pathway after a 38-day FDA review.

K961853 · Acufex Microsurgical, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 1996
Decision
38d
Days
Class 2
Risk

K961853 is an FDA 510(k) clearance for the PROLINE FAST PASS ARTHOSCOPIC NEEDLE PASSER. Classified as Arthroscope (product code HRX), Class II - Special Controls.

Submitted by Acufex Microsurgical, Inc. (Mansfield, US). The FDA issued a Cleared decision on June 21, 1996 after a review of 38 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 888.1100 - the FDA general and plastic surgery device 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 Acufex Microsurgical, Inc. devices

FDA 510(k) Submission Details - K961853

510(k) Number K961853 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 14, 1996
Decision Date June 21, 1996
Days to Decision 38 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
77d faster than avg
Panel avg: 115d · This submission: 38d
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 General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - HRX Arthroscope

All 520
Devices cleared under the same product code (HRX) and FDA review panel - the closest regulatory comparables to K961853.
ARTHRO-SURGIMAT
K962114 · W.O.M. World of Medicine GmbH · Aug 1996
ARTHOCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970
K962321 · Arthrocare Corp. · Jul 1996
ARTHROCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM (MODEL 970)
K961747 · Arthrocare Corp. · Jul 1996
INSTRUMENT SET FOR ARTHROSCOPIC PERCUTANEOUS DISCECTOMY
K961713 · KARL STORZ Endoscopy-America, Inc. · May 1996
KSEA INSTRUMENTS FOR ENDOSCOPIC TREATMENT OF CARPAL TUNNEL SYNDROME
K961244 · KARL STORZ Endoscopy-America, Inc. · May 1996
ARTHOSCOPE
K960805 · United States Surgical, A Division of Tyco Healthc · Apr 1996