Cleared Traditional

K970897 - BTI DISTAL FEMORAL INTRAMEDULLARY ROD S...

K970897 is an FDA 510(k) clearance for BTI DISTAL FEMORAL INTRAMEDULLARY ROD S..., manufactured by Biodynamic Technologies, Inc.. The device is a Class 2 Orthopedic device with product code HSB cleared through the Traditional 510(k) pathway after a 41-day FDA review.

K970897 · Biodynamic Technologies, Inc. · Orthopedic device
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Apr 1997
Decision
41d
Days
Class 2
Risk

K970897 is an FDA 510(k) clearance for the BTI DISTAL FEMORAL INTRAMEDULLARY ROD SYSTEM. Classified as Rod, Fixation, Intramedullary And Accessories (product code HSB), Class II - Special Controls.

Submitted by Biodynamic Technologies, Inc. (Deerfield Beach, US). The FDA issued a Cleared decision on April 21, 1997 after a review of 41 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3020 - 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 Biodynamic Technologies, Inc. devices

FDA 510(k) Submission Details - K970897

510(k) Number K970897 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 11, 1997
Decision Date April 21, 1997
Days to Decision 41 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
81d faster than avg
Panel avg: 122d · This submission: 41d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HSB Device Classification - Class 2, Special Controls

Product Code HSB Rod, Fixation, Intramedullary And Accessories
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3020
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 - HSB Rod, Fixation, Intramedullary And Accessories

All 365
Devices cleared under the same product code (HSB) and FDA review panel - the closest regulatory comparables to K970897.
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K970280 · Ferguson Medical · May 1997
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K961360 · Encore Orthopedics, Inc. · Mar 1997
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K965098 · Zimmer, Inc. · Feb 1997
TRIMAX NAIL SYSTEM
K964163 · Smith & Nephew Richards, Inc. · Dec 1996