Cleared Traditional

K955480 - BOZOTTA REINSERTION FORCEPS

K955480 is the FDA 510(k) clearance for BOZOTTA REINSERTION FORCEPS by KARL STORZ Endoscopy-America, Inc.. It is a Class 2 Orthopedic device (product code HRX) cleared through the Traditional 510(k) pathway after a 71-day FDA review.

K955480 · KARL STORZ Endoscopy-America, Inc. · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1996
Decision
71d
Days
Class 2
Risk

K955480 is an FDA 510(k) clearance for the BOZOTTA REINSERTION FORCEPS. Classified as Arthroscope (product code HRX), Class II - Special Controls.

Submitted by KARL STORZ Endoscopy-America, Inc. (Culver City, US). The FDA issued a Cleared decision on February 9, 1996 after a review of 71 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 KARL STORZ Endoscopy-America, Inc. devices

Submission Details

510(k) Number K955480 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 30, 1995
Decision Date February 09, 1996
Days to Decision 71 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
51d faster than avg
Panel avg: 122d · This submission: 71d
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 K955480.
ARTHOSCOPE
K960805 · United States Surgical, A Division of Tyco Healthc · Apr 1996
PERCUTANEOUS ENDOSCOPIC DISCECTOMY
K960222 · Richard Wolf Medical Instruments Corp. · Mar 1996
AESCULAP ENDOSCCOPIC SPINE INSTRUMENTS
K954652 · Aesculap, Inc. · Feb 1996
KARL STORZ TARGETING UNIT
K955652 · KARL STORZ Endoscopy-America, Inc. · Jan 1996
INCL ENDOSCOPE
K955471 · Sofamor Danek USA,Inc. · Dec 1995
CANNULOC THREADED CANNULA
K955273 · Linvatec Corp. · Dec 1995