Cleared Traditional

K874911 - MCCAIN INSTRUMENT TMJ/SM. JOINT ARTHROS...

K874911 is the FDA 510(k) clearance for MCCAIN INSTRUMENT TMJ/SM. JOINT ARTHROS... by Walter Lorenz Surgical, Inc.. It is a Class 2 Orthopedic device (product code HRX) cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K874911 · Walter Lorenz Surgical, Inc. · Orthopedic device
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Feb 1988
Decision
84d
Days
Class 2
Risk

K874911 is an FDA 510(k) clearance for the MCCAIN INSTRUMENT TMJ/SM. JOINT ARTHROSCOPIC SURG. Classified as Arthroscope (product code HRX), Class II - Special Controls.

Submitted by Walter Lorenz Surgical, Inc. (Jacksonville, US). The FDA issued a Cleared decision on February 24, 1988 after a review of 84 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 Walter Lorenz Surgical, Inc. devices

Submission Details

510(k) Number K874911 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 02, 1987
Decision Date February 24, 1988
Days to Decision 84 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
38d faster than avg
Panel avg: 122d · This submission: 84d
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 361
Devices cleared under the same product code (HRX) and FDA review panel - the closest regulatory comparables to K874911.
3M CARPAL TUNNEL
K881703 · 3M Company · Jul 1988
HERMAN CANNULA SET
K880203 · Orthopedic Systems, Inc. · Apr 1988
TENDON HARVESTER
K880414 · Concept, Inc. · Mar 1988
ORTHO. GAS INSUFFLATOR MODEL IN-2 FOR ARTHRO. SURG
K873331 · Directed Energy, Inc. · Feb 1988
EDWARDS ORTHOPAEDICS ARTHROSCOPES AND ACCESSORIES
K880205 · Baxter Healthcare Corp · Feb 1988
CONCEPT SUTURE NEEDLE
K874515 · Concept, Inc. · Nov 1987