Cleared Traditional

K993736 - EXACTECH ACUMATCH INTEGRATED HIP SYSTEM...

K993736 is the FDA 510(k) clearance for EXACTECH ACUMATCH INTEGRATED HIP SYSTEM... by Exactech, Inc.. It is a Class 2 Orthopedic device (product code LPH) cleared through the Traditional 510(k) pathway after a 77-day FDA review.

K993736 · Exactech, Inc. · Orthopedic device
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Jan 2000
Decision
77d
Days
Class 2
Risk

K993736 is an FDA 510(k) clearance for the EXACTECH ACUMATCH INTEGRATED HIP SYSTEM M-SERIES FEMORAL STEM COMPONENT. Classified as Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented (product code LPH), Class II - Special Controls.

Submitted by Exactech, Inc. (Gainesville, US). The FDA issued a Cleared decision on January 20, 2000 after a review of 77 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3358 - 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 Exactech, Inc. devices

Submission Details

510(k) Number K993736 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 04, 1999
Decision Date January 20, 2000
Days to Decision 77 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
45d faster than avg
Panel avg: 122d · This submission: 77d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code LPH Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3358
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 - LPH Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented

All 446
Devices cleared under the same product code (LPH) and FDA review panel - the closest regulatory comparables to K993736.
IMPACT MODULAR TOTAL HIP SYSTEM
K000334 · Biomet, Inc. · Feb 2000
POROCOAT PRODIGY HIP PROSTHESIS
K000207 · DePuy Orthopaedics, Inc. · Feb 2000
MARATHON CROSS-LINKED POLYETHYLENE ACETABULAR CUP LINERS
K994415 · DePuy Orthopaedics, Inc. · Feb 2000
REVELATION POROUS HIP STEM
K994070 · Encore Orthopedics, Inc. · Jan 2000
MODULAR REACH HIP
K994038 · Biomet, Inc. · Dec 1999
DURATION IV STERILIZATION PROCESS (ACETABULAR INSERTS)
K990849 · Howmedica Osteonics Corp. · Dec 1999