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

BIOGLASS DENTAL ENDOSSEOUS RIDGE MAINTAINER

K Number: K880371 · Decision Nov 18, 1988
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
229
Applicant Total
6
Review Days
296

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
BIOGLASS DENTAL ENDOSSEOUS RIDGE MAINTAINER
K Number
K880371
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
American Biomaterials Corp.
Date Received
January 27, 1988
Decision Date
November 18, 1988
Product Code
LYC
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
LYC Bone Grafting Material, Synthetic

Similar 510(k) Clearances

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

View all

Other Clearances by American Biomaterials Corp.

K Number Device Name
K922455 EVERT-O-CATH CATHETER
K924725 AMERICAN BIOMED, INC. MICROSURGICAL INSTRUMENTS
K915824 HOLE PUNCH
K863796 CREATIVE CARE SYSTEMS' IV START KIT
K843461 BIOGLASS OSSICULAR RECONSTRUCTION PROSTH