Cleared Traditional

K062712 - ERBE MONOPOLAR ATTACHMENT FOR HELIX HYD...

K062712 is the FDA 510(k) clearance for ERBE MONOPOLAR ATTACHMENT FOR HELIX HYD... by Erbe USA, Inc.. It is a Class 2 General & Plastic Surgery device (product code GEI) cleared through the Traditional 510(k) pathway after a 137-day FDA review.

K062712 · Erbe USA, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 2007
Decision
137d
Days
Class 2
Risk

K062712 is an FDA 510(k) clearance for the ERBE MONOPOLAR ATTACHMENT FOR HELIX HYDRO-JET, MODEL P/N 20139-094. Classified as Electrosurgical, Cutting & Coagulation & Accessories within the GEI classification (a category for electrosurgical cutting and coagulation devices), Class II - Special Controls.

Submitted by Erbe USA, Inc. (Marietta, US). The FDA issued a Cleared decision on January 26, 2007 after a review of 137 days - within the typical 510(k) review window.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4400 - 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 Erbe USA, Inc. devices

Submission Details

510(k) Number K062712 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 11, 2006
Decision Date January 26, 2007
Days to Decision 137 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
22d slower than avg
Panel avg: 115d · This submission: 137d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GEI Electrosurgical, Cutting & Coagulation & Accessories
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4400
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 - GEI Electrosurgical, Cutting & Coagulation & Accessories

All 1130
Devices cleared under the same product code (GEI) and FDA review panel - the closest regulatory comparables to K062712.
MODIFICATION TO ARTHROCARE ARTHROWANDS
K070958 · Arthrocare Corp. · Apr 2007
ARTHROCARE SPINEWANDS
K070851 · Arthrocare Corp. · Apr 2007
MODIFICATION TO AUTOCON II 400 ELECTROSURGICAL GENERATOR
K062464 · KARL STORZ Endoscopy-America, Inc. · Feb 2007
ATRICURE ABLATION SYSTEM
K063630 · AtriCure, Inc. · Jan 2007
CONMED ABC DISSECTING BLADE ELECTRODE, MODEL 139330
K062082 · Conmed Corporation · Jan 2007
ARTHROCARE CONTROLLER (SYSTEM 2000 AND 8000), ARTHROCARE PATIENT CABLE, FOOT CONTROL, POWER CORD AND WANDS
K063538 · Arthrocare Corp. · Dec 2006