Cleared Traditional

K800142 - FUSON BONE PLUG

K800142 is an FDA 510(k) clearance for FUSON BONE PLUG, manufactured by Zimmer, Inc.. The device is a Class 2 Orthopedic device with product code JDS cleared through the Traditional 510(k) pathway after a 29-day FDA review.

K800142 · Zimmer, Inc. · Orthopedic device
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Feb 1980
Decision
29d
Days
Class 2
Risk

K800142 is an FDA 510(k) clearance for the FUSON BONE PLUG, RADIOPAQUE. Classified as Nail, Fixation, Bone (product code JDS), Class II - Special Controls.

Submitted by Zimmer, Inc. (Walker, US). The FDA issued a Cleared decision on February 19, 1980 after a review of 29 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3030 - 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 Zimmer, Inc. devices

FDA 510(k) Submission Details - K800142

510(k) Number K800142 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 21, 1980
Decision Date February 19, 1980
Days to Decision 29 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
93d faster than avg
Panel avg: 122d · This submission: 29d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JDS Device Classification - Class 2, Special Controls

Product Code JDS Nail, Fixation, Bone
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3030
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 - JDS Nail, Fixation, Bone

All 38
Devices cleared under the same product code (JDS) and FDA review panel - the closest regulatory comparables to K800142.
HUMERAL LOCKING NAIL SYSTEM
K883882 · Howmedica Corp. · Jan 1989
INTRAMEDULLARY BONE PLUG
K832328 · Kirschner Medical Corp. · Oct 1983
SILASTIC BONE PLUG H.P.(CEMENT RESTRICT)
K800898 · Dow Corning Corp. Healthcare Industries Materials · May 1980
FEMORAL CEMENT RESTRICTOR
K800144 · Biomet, Inc. · Feb 1980
B.G. FLEXIBLE NAIL SYSTEM
K770130 · Howmedica Corp. · Jan 1977