FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ProCinch Adjustable Loop Device

K Number: K150416 · Decision Apr 17, 2015
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
101
Review Days
58

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ProCinch Adjustable Loop Device
K Number
K150416
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Endoscopy
Date Received
February 18, 2015
Decision Date
April 17, 2015
Product Code
HTY
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HTY Pin, Fixation, Smooth

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HTY), ordered by most recent decision date.

View all

Other Clearances by Stryker Endoscopy

K Number Device Name
K253602 Precision S 4K Sinuscope
K261037 780 nm SPY Portable Handheld Imaging (SPY-PHI) System
K260185 1688 4K Camera System with Advanced Imaging Modality; 1788 4K Camera System with Advanced Imaging Modality
K260108 L12 LED Light Source with AIM
K254014 Connected OR Hub with Device and Voice Control; SDC4K Information Management System with Device and Voice Control
K253888 MOLLI 2 System
K252010 SPY Laparoscope
K252012 SPY Cystoscope/Hysteroscope
K250544 Knotilus+ Biocomposite Knotless Anchor
K250528 Stryker AlphaVent™ Knotless SP Biocomposite Anchor
Search all 101 clearances from Stryker Endoscopy →