510(k) K972317

MONTGOMERY THYROPLASTY IMPLANT SYSTEM by Boston Medical Products, Inc. — Product Code MIX

K972317 is an FDA 510(k) premarket notification submitted by Boston Medical Products, Inc. for the device "MONTGOMERY THYROPLASTY IMPLANT SYSTEM". The FDA issued a decision of Substantially Equivalent on September 18, 1997. The device falls under product code MIX (System, Vocal Cord Medialization), a Class II device regulated under 21 CFR 874.3620. Boston Medical Products, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 18, 1997
Date Received
June 20, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Vocal Cord Medialization
Device Class
Class II
Regulation Number
874.3620
Review Panel
EN
Submission Type