Cleared Traditional

K091207 - SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (...

K091207 is the FDA 510(k) clearance for SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (... by Surgicraft , Ltd.. It is a Class 2 Orthopedic device (product code HTN) cleared through the Traditional 510(k) pathway after a 662-day FDA review.

K091207 · Surgicraft , Ltd. · Orthopedic device
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Optimized for regulatory review, auditing and printing
Feb 2011
Decision
662d
Days
Class 2
Risk

K091207 is an FDA 510(k) clearance for the SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (AC) DEVICE. Classified as Washer, Bolt Nut (product code HTN), Class II - Special Controls.

Submitted by Surgicraft , Ltd. (Douglassville, US). The FDA issued a Cleared decision on February 15, 2011 after a review of 662 days - an unusually long review period, suggesting complex equivalence evaluation.

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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Orthopedic submissions.

View all Surgicraft , Ltd. devices

Submission Details

510(k) Number K091207 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 24, 2009
Decision Date February 15, 2011
Days to Decision 662 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
540d slower than avg
Panel avg: 122d · This submission: 662d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code HTN Washer, Bolt Nut
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 - HTN Washer, Bolt Nut

All 66
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