Cleared Traditional

K905112 - SNAP-PAK (TM)

K905112 is an FDA 510(k) clearance for SNAP-PAK (TM), manufactured by Mitek Surgical Products, Inc.. The device is a Class 2 Orthopedic device with product code JDR cleared through the Traditional 510(k) pathway after a 52-day FDA review.

K905112 · Mitek Surgical Products, Inc. · Orthopedic device
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Jan 1991
Decision
52d
Days
Class 2
Risk

K905112 is an FDA 510(k) clearance for the SNAP-PAK (TM). Classified as Staple, Fixation, Bone (product code JDR), Class II - Special Controls.

Submitted by Mitek Surgical Products, Inc. (Norwood, US). The FDA issued a Cleared decision on January 4, 1991 after a review of 52 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 Mitek Surgical Products, Inc. devices

FDA 510(k) Submission Details - K905112

510(k) Number K905112 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 13, 1990
Decision Date January 04, 1991
Days to Decision 52 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
70d faster than avg
Panel avg: 122d · This submission: 52d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JDR Device Classification - Class 2, Special Controls

Product Code JDR Staple, 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 - JDR Staple, Fixation, Bone

All 197
Devices cleared under the same product code (JDR) and FDA review panel - the closest regulatory comparables to K905112.
MITEK ANCHOR, MITEK ANCHOR II
K920213 · Mitek Surgical Products, Inc. · May 1992
SURETAC POLYGLYCONATE ABSORBABLE FIXATION DEVICE
K911837 · Acufex Microsurgical, Inc. · Nov 1991
BIODEGRADABLE SURGICAL STAPLE
K910723 · Instrument Makar, Inc. · Mar 1991
BONE STAPLE(S)
K904553 · Synthes (Usa) · Dec 1990
BARBED SQUARE STAPLE
K905362 · O'Tec Corp. · Dec 1990
FIXATION STAPLE
K905363 · O'Tec Corp. · Dec 1990