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

Monosyn Quick Synthetic Absorbable Surgical Suture

K Number: K171001 · Decision Oct 23, 2017
Classifications
1
FEI Numbers
140
Registration Numbers
140
Same Product Code
147
Applicant Total
207
Review Days
202

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
Monosyn Quick Synthetic Absorbable Surgical Suture
K Number
K171001
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4493
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aesculap, Inc.
Date Received
April 4, 2017
Decision Date
October 23, 2017
Product Code
GAM
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GAM Suture, Absorbable, Synthetic, Polyglycolic Acid

Similar 510(k) Clearances

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

View all

Other Clearances by Aesculap, Inc.

K Number Device Name
K242762 Aesculap Aicon® Series Container System
K242003 XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter Set
K223596 SQ.line KERRISON
K214041 Aesculap AICON Container
K211572 Aesculap Slim Clip Applier
K203739 ELAN 4 Electro Motor System
K202391 DIR 800
K203461 Aesculap Caiman 12 Seal and Cut Technology System
K202938 Aesculap Caiman 5 Seal and Cut Technology System
K202124 Aesculap PAS-Port Proximal Anastomosis System
Search all 207 clearances from Aesculap, Inc. →