Cleared Traditional

K930617 - OBGRIP AND UNITIPS(TM)

K930617 is an FDA 510(k) clearance for OBGRIP AND UNITIPS(TM), manufactured by Unisurge, Inc.. The device is a Class 2 General & Plastic Surgery device with product code GCJ cleared through the Traditional 510(k) pathway after a 184-day FDA review.

K930617 · Unisurge, Inc. · General & Plastic Surgery device
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Aug 1993
Decision
184d
Days
Class 2
Risk

K930617 is an FDA 510(k) clearance for the OBGRIP AND UNITIPS(TM). Classified as Laparoscope, General & Plastic Surgery (product code GCJ), Class II - Special Controls.

Submitted by Unisurge, Inc. (Cupertino, US). The FDA issued a Cleared decision on August 11, 1993 after a review of 184 days - an extended review 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Unisurge, Inc. devices

FDA 510(k) Submission Details - K930617

510(k) Number K930617 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 08, 1993
Decision Date August 11, 1993
Days to Decision 184 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
69d slower than avg
Panel avg: 115d · This submission: 184d
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 1096
Devices cleared under the same product code (GCJ) and FDA review panel - the closest regulatory comparables to K930617.
SRUGICAL RETRACTOR, MODIFICATION
K933049 · Advanced Surgical, Inc. · Aug 1993
IMAGYN MEDICAL VIDEOSCOPY SYST W/IRRIG PUMP & ACCE
K931518 · Imagyn Medical, Inc. · Aug 1993
SURGICAL TROCAR AND TROCAR SLEEVE
K932229 · Origin Medsystems, Inc. · Aug 1993
REUSABLE ENDOSCOPIC SCISSORS, GRASPER-MONOPOLAR
K926583 · T. Korossurgical Instruments Corp. · Aug 1993
REUSABLE/INTERCHANGEABLE SHAFT, ENDOSCOPIC SCISSOR
K931262 · T. Korossurgical Instruments Corp. · Aug 1993
LAPAROSCOPIC BALLOON RETRACTOR
K931649 · Cabot Medical Corp. · Aug 1993