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

CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR, MODEL C6170CR

K Number: K090835 · Decision Jun 22, 2009
Classifications
1
FEI Numbers
140
Registration Numbers
140
Same Product Code
213
Applicant Total
93
Review Days
87

Basic Information

Device Name
CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR, MODEL C6170CR
K Number
K090835
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
LINVATEC CORP.
Date Received
March 27, 2009
Decision Date
June 22, 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 LINVATEC CORP.

K Number Device Name
K092998 CONMED LINVATEC INTERCEPT IMPLANT
K091549 CONMED LINVATEC SOFT TISSUE TO BONE SYSTEM
K090186 CONMED LINVATEC PALADIN, PRELOADED WITH TWO #2 HI-FI SUTURES
K083281 EL LIGHTWAVE SUCTION ABLATOR, MODEL EL-2000-S, LIGHTWAVE SUCTION ABLATOR, MODEL IA-2000-S, LIGHTWAVE ABLATOR, MODEL IA-
K060198 MICROPOWER HAND PIECE : MEDIUM SPEED DRILL, SAGGITAL SAW, RECIPROCATING SAW, AND OSCILLATING SAW
K060270 MICROPOWER HAND PIECE: ORAL MAX HIGH SPEED DRILL
K060260 MICROPOWER HAND PIECE HIGH SPEED DRILL
K050519 ADVANCED TURBO DRIVE SYSTEM
K050497 BIOSCREW XTRALOK, 8X35MM & 8X40MM VIOLET
K050227 THREVO SUTURE ANCHOR WITH DISPOSABLE DRIVER
Search all 93 clearances from LINVATEC CORP. →