Atlas FDA

Hintermann Series H3 Total Ankle Replacement System

FDA premarket approval P160036/S003 · decided 2021-10-15

Approval details

PMA number
P160036
Supplement
S003
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
Trade name
Hintermann Series H3 Total Ankle Replacement System
Generic name
Prosthesis, ankle, uncemented, non-constrained
Applicant
Dt Medtech, LLC
Date received
2021-09-10
Decision date
2021-10-15
Days to decision
35 days
Decision code
APPR
Product code
NTG
Advisory committee
Orthopedic
Expedited review
No
Location
Towson, MD
Statement
Approval of the revised protocol for the post-approval study (PAS) protocol.

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510(k) clearances by this applicant

RecordFirmDate
Hintermann Series H2 Total Ankle System (K171004)Dt Medtech, LLC2017-11-07