Cleared Traditional

K932041 - XANCHOR SUTURE ATTACHMENT DEVICE

K932041 is an FDA 510(k) clearance for XANCHOR SUTURE ATTACHMENT DEVICE, manufactured by Orthopaedic Biosystems. The device is a Class 2 Orthopedic device with product code JDR cleared through the Traditional 510(k) pathway after a 472-day FDA review.

K932041 · Orthopaedic Biosystems · Orthopedic device
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Aug 1994
Decision
472d
Days
Class 2
Risk

K932041 is an FDA 510(k) clearance for the XANCHOR SUTURE ATTACHMENT DEVICE. Classified as Staple, Fixation, Bone (product code JDR), Class II - Special Controls.

Submitted by Orthopaedic Biosystems (Mesa, US). The FDA issued a Cleared decision on August 12, 1994 after a review of 472 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 Orthopaedic Biosystems devices

FDA 510(k) Submission Details - K932041

510(k) Number K932041 FDA.gov
FDA Decision Cleared Substantially Equivalent - NSE Converted (SN)
Date Received April 27, 1993
Decision Date August 12, 1994
Days to Decision 472 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
350d slower than avg
Panel avg: 122d · This submission: 472d
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 211
Devices cleared under the same product code (JDR) and FDA review panel - the closest regulatory comparables to K932041.
ARTHREX STAPLES
K943492 · Arthrex, Inc. · Feb 1995
BONE ANCHOR
K942787 · Acu Med, Inc. · Dec 1994
INNOVASIVE SUTURE BONE FASTENER WITH SUTURE
K935321 · Innovasive Devices, Inc. · Oct 1994
MITEK GIII ANCHOR
K931782 · Mitek Surgical Products, Inc. · Jul 1994
QUICKANCHOR II
K931253 · Mitek Surgical Products, Inc. · Jun 1994
ACUFEX SURETAC
K931519 · Acufex Microsurgical, Inc. · Jun 1994