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

CONMED LINVATEC PRESTO PRELOADED WITH ONE OR TWO #2 HI-FI SUTURES

K Number: K092898 · Decision Oct 19, 2009
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
219
Applicant Total
21
Review Days
28

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
CONMED LINVATEC PRESTO PRELOADED WITH ONE OR TWO #2 HI-FI SUTURES
K Number
K092898
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Conmed Linvatec
Date Received
September 21, 2009
Decision Date
October 19, 2009
Product Code
MAI
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
MAI Fastener, Fixation, Biodegradable, Soft Tissue

Similar 510(k) Clearances

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

View all

Other Clearances by Conmed Linvatec

K Number Device Name
K111779 Y-KNOT ALL-SUTURE ANCHOR MODEL HF13
K102410 MATRYX INTERFERENCE SCREW (5.0-6.5MM)
K102339 CONMED LINVATEC SEQUENT MENISCAL REPAIR DEVICE
K101100 CROSSFT OC SUTURE ANCHOR MODE CFC-4502, CFC-5502, CFC-6502, CFC-4503, CFC-5503, CFC-6503
K090560 CONMED LINVATEC ANODIZED ALUMINUM STERILIZATION TRAYS
K083161 ZEN WIRELESS FOOTSWITCH (W1000), ZEN WIRELESS FOOTSWITCH ADAPTER (W1100)
K080531 CONMED LINVATEC MICROFRACTURE INSTRUMENT STERILIZATION TRAY
K072291 CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR
K080444 CONMED LINVATEC OSPREY DRILL SYSTEM
K073481 THREVO ANCHOR, DISPOSABLE DRIVER, HI-FI SUTURES
Search all 21 clearances from Conmed Linvatec →