Cleared Traditional

K992369 - SYNERGY INTEGRAL SCREWS, MODELS, 2161,2162,2163,2164,2165,2166,2167,2168,2169,2210,2211,2212,2215,2216,2217,2220,2221,22

K992369 is an FDA 510(k) clearance for SYNERGY INTEGRAL SCREWS, manufactured by Interpore Cross Intl.. The device is a Class 2 Orthopedic device with product code MNI cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K992369 · Interpore Cross Intl. · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 1999
Decision
90d
Days
Class 2
Risk

K992369 is an FDA 510(k) clearance for the SYNERGY INTEGRAL SCREWS, MODELS, 2161,2162,2163,2164,2165,2166,2167,2168,2169.... Classified as Orthosis, Spinal Pedicle Fixation (product code MNI), Class II - Special Controls.

Submitted by Interpore Cross Intl. (Irvine, US). The FDA issued a Cleared decision on October 13, 1999 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3070 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Orthopedic review framework, consistent with the majority of Class II 510(k) submissions.

View all Interpore Cross Intl. devices

FDA 510(k) Submission Details - K992369

510(k) Number K992369 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 15, 1999
Decision Date October 13, 1999
Days to Decision 90 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
32d faster than avg
Panel avg: 122d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MNI Device Classification - Class 2, Special Controls

Product Code MNI Orthosis, Spinal Pedicle Fixation
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3070
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 - MNI Orthosis, Spinal Pedicle Fixation

All 275
Devices cleared under the same product code (MNI) and FDA review panel - the closest regulatory comparables to K992369.
EBI SPINELINK SYSTEM
K992920 · Ebi, L.P. · Nov 1999
ISOBAR SEMI-RIGID SPINAL SYSTEM
K991326 · Scien'Tx USA, Inc. · Nov 1999
ISOBAR SPINAL SYSTEM
K992738 · Encore Orthopedics, Inc. · Nov 1999
EBI OMEGA 21 SYSTEM
K992333 · Electro-Biology, Inc. · Oct 1999
MODIFICATION TO SILHOUETTE SPINAL FIXATION SYSTEM
K992276 · Sulzer Spine-Tech · Oct 1999
CD HORIZON SPINAL SYSTEM
K992928 · Sofamor Danek USA,Inc. · Sep 1999