Cleared Traditional

K951252 - KARL STORZ PEDIATRIC PYLORIC SPREADER

K951252 is the FDA 510(k) clearance for KARL STORZ PEDIATRIC PYLORIC SPREADER by KARL STORZ Endoscopy-America, Inc.. It is a Class 2 General & Plastic Surgery device (product code GCJ) cleared through the Traditional 510(k) pathway after a 36-day FDA review.

K951252 · KARL STORZ Endoscopy-America, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 1995
Decision
36d
Days
Class 2
Risk

K951252 is an FDA 510(k) clearance for the KARL STORZ PEDIATRIC PYLORIC SPREADER, PYLOROTOME, ENDOTOME. Classified as Laparoscope, General & Plastic Surgery (product code GCJ), Class II - Special Controls.

Submitted by KARL STORZ Endoscopy-America, Inc. (Culver City, US). The FDA issued a Cleared decision on April 25, 1995 after a review of 36 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 KARL STORZ Endoscopy-America, Inc. devices

Submission Details

510(k) Number K951252 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 20, 1995
Decision Date April 25, 1995
Days to Decision 36 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
79d faster than avg
Panel avg: 115d · This submission: 36d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 693
Devices cleared under the same product code (GCJ) and FDA review panel - the closest regulatory comparables to K951252.
KARL STORZ ENDOSCOPES, TELESCOPE HOLDERS
K951535 · KARL STORZ Endoscopy-America, Inc. · May 1995
CCD ENDOCAM 5501
K950502 · Richard Wolf Medical Instruments Corp. · May 1995
ENDOSCOPES AND ACCESSORIES
K950612 · Storz Instrument Co. · Apr 1995
ENDOPATH OPTICAL ACCESS NEEDKLE
K951444 · Ethicon Endo-Surgery, Inc. · Apr 1995
SYMBIOSIS BIPOLAR SCISSORS
K951387 · Symbiosis Corp. · Apr 1995
KSEA STEINER ELECTROMECHANIC MORCELLATOR
K950339 · KARL STORZ Endoscopy-America, Inc. · Apr 1995