Cleared Traditional

K013090 - SOPRO 67D OPERATING ROOM CAMERA

K013090 is an FDA 510(k) clearance for SOPRO 67D OPERATING ROOM CAMERA, manufactured by Sopro. The device is a Class 2 General & Plastic Surgery device with product code GCJ cleared through the Traditional 510(k) pathway after a 87-day FDA review.

K013090 · Sopro · General & Plastic Surgery device
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Dec 2001
Decision
87d
Days
Class 2
Risk

K013090 is an FDA 510(k) clearance for the SOPRO 67D OPERATING ROOM CAMERA. Classified as Laparoscope, General & Plastic Surgery (product code GCJ), Class II - Special Controls.

Submitted by Sopro (Marseille, FR). The FDA issued a Cleared decision on December 13, 2001 after a review of 87 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 876.1500 - the FDA general and plastic surgery device 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 Sopro devices

FDA 510(k) Submission Details - K013090

510(k) Number K013090 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 17, 2001
Decision Date December 13, 2001
Days to Decision 87 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
28d faster than avg
Panel avg: 115d · This submission: 87d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GCJ Device Classification - Class 2, Special Controls

Product Code GCJ Laparoscope, General & Plastic Surgery
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1500
Definition Validated Reprocessing Instructions And Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission If The Device Is Reusable And Has Specific Design Features (please Refer To Table 2 Of 82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf).
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 General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - GCJ Laparoscope, General & Plastic Surgery

All 724
Devices cleared under the same product code (GCJ) and FDA review panel - the closest regulatory comparables to K013090.
DILATING TIP OBTURATOR
K012884 · Applied Medical Resources Corp. · Jan 2002
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K014250 · Guidant Corp. · Jan 2002
APPLIED ACCESS SEAL
K012968 · Applied Medical Resources Corp. · Dec 2001
KSEA SIALOENDOSCOPES AND ACCESSORIES
K012527 · KARL STORZ Endoscopy-America, Inc. · Nov 2001
DYONICS VISION 635 DIGITAL CAPTURE SYSTEM, MODEL 7209088
K011944 · Smith & Nephew, Inc. · Sep 2001