# K092377: Plastic Temporary Abutments, Models: PT341S, PT344S, PT341A, PT344A, PT451S, PT454S, PT451A, PT454A, PT561S, PT564S

- Pathway: 510(k) (Traditional)
- Applicant: Zimmer Dental, Inc.
- Decided: Nov 3, 2009 after 90 days
- Product code: NHA (Abutment, Implant, Dental, Endosseous)
- Device class: 2
- Regulation: 21 CFR 872.3630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
51 later devices descend from it; 7 cite it directly.
0 of 52 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Hex-Lock® Temporary Abutment: named in the summary without a submission number
- (no number) Friadent® EsthetiCap: named in the summary without a submission number
- (no number) PreFormance Post: named in the summary without a submission number

## Most influential descendants
- K132125: A.B. Dental Devices Dental Implants System (2014), 25 descendants of its own
- K112099: Contour Healer (2012), 21 descendants of its own
- K120793: Z-LOOK3 Evo SLM (2012), 19 descendants of its own
- K140440: Noris Medical Dental Implants System (2014), 14 descendants of its own
- K151328: PURE Ceramic Implants (2016), 12 descendants of its own

## Indications for use
The Plastic Temporary Abutment is intended to be used to fabricate and support provisional restorations that aid in creating an esthetic emergence through the gingiva during the healing period and prior to final restoration. The Plastic Temporary Abutment can be used for cement-retained or screw-retained provisional restorations. The abutments can be used for single-unit and multi-unit restorations. Use of the Plastic Temporary Abutment is not to exceed one-hundred and eighty (180) days.

Source page: https://510kreport.com/device/K092377
Methodology: https://510kreport.com/methodology