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

BIO-OSS, BIO-OSS BLOCKS AND BIO-OSS COLLAGEN

K Number: K033815 · Decision Jan 15, 2004
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
39
Applicant Total
16
Review Days
37

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Basic Information

Device Name
BIO-OSS, BIO-OSS BLOCKS AND BIO-OSS COLLAGEN
K Number
K033815
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Geistlich-Pharma
Date Received
December 9, 2003
Decision Date
January 15, 2004
Product Code
NPM
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
NPM Bone Grafting Material, Animal Source

Similar 510(k) Clearances

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

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Other Clearances by Geistlich-Pharma

K Number Device Name
K014289 ORTHOSS RESORBABLE BONE VOID FILLER
K970569 BIO-BLOCKS
K974399 BIO-OSS COLLAGEN
K970321 BIO-OSS ANORGANIC BOVINE BONE
K972817 RESOR-PIN RESORBABLE MEMBRANE PIN
K960724 BIO-GIDE RESORBABLE BILAYER MEMBRANE
K952619 BIO-OSS CERAMIC
K952618 BIO-OSS
K952617 BIO-OSS
K920508 BIO-OSS BLOCKS
Search all 16 clearances from Geistlich-Pharma →